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Volumn , Issue , 2008, Pages 273-309

Hair loss in children

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EID: 84892304857     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-540-46911-7_14     Document Type: Chapter
Times cited : (12)

References (108)
  • 1
    • 6844265562 scopus 로고    scopus 로고
    • Alopecia universalis associated with a mutation in the human hairless gene
    • Ahmad W, Faiyaz ul Haque M, Brancolini V et al (1998) Alopecia universalis associated with a mutation in the human hairless gene. Science 279: 720-724.
    • (1998) Science , vol.279 , pp. 720-724
    • Ahmad, W.1    Faiyaz, U.H.M.2    Brancolini, V.3
  • 2
    • 0033210613 scopus 로고    scopus 로고
    • Molecular basis of congenital atrichia in humans and mice
    • Ahmad W, Panteleyev A, Christiano AM (1999) Molecular basis of congenital atrichia in humans and mice. Cutis 64: 269-276.
    • (1999) Cutis , vol.64 , pp. 269-276
    • Ahmad, W.1    Panteleyev, A.2    Christiano, A.M.3
  • 3
    • 0036829167 scopus 로고    scopus 로고
    • Two brothers with keratosis follicularis spinulosa decalvans
    • Alfadley A, Al Hawsawi K, Hainau B et al (2002) Two brothers with keratosis follicularis spinulosa decalvans. J Am Acad Dermatol 47: 275-278.
    • (2002) J Am Acad Dermatol , vol.47 , pp. 275-278
    • Alfadley, A.1    Al, H.K.2    Hainau, B.3
  • 4
    • 3042687028 scopus 로고
    • J. Pili torti hereditaria
    • Appel B, Messina S (1942) J.Pili torti hereditaria. New Eng J Med 226: 912-915.
    • (1942) New Eng J Med , vol.226 , pp. 912-915
    • Appel, B.1    Messina, S.2
  • 6
    • 0028345136 scopus 로고
    • Clinical findings, cutaneous pathology, and response to therapy in 21 patients with keratosis pilaris atrophicans
    • Baden HP, Byers HR (1994) Clinical findings, cutaneous pathology, and response to therapy in 21 patients with keratosis pilaris atrophicans. Arch Dermatol 130:469-475.
    • (1994) Arch Dermatol , vol.130 , pp. 469-475
    • Baden, H.P.1    Byers, H.R.2
  • 7
    • 0142241935 scopus 로고    scopus 로고
    • The hair in infancy and childhood
    • Rook A, Dawber R (eds), Blackwell Science London
    • Barth JH (2005) The hair in infancy and childhood. In: Rook A, Dawber R (eds) Disease of the hair and scalp. Blackwell Science London. pp 51-56.
    • (2005) Disease of the Hair and Scalp , pp. 51-56
    • Barth, J.H.1
  • 8
    • 0034123513 scopus 로고    scopus 로고
    • An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family
    • Baumer A, Belli S, Trueb RM, Schinzel A (2000) An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family. Eur J Hum Genet 8: 443-448.
    • (2000) Eur J Hum Genet , vol.8 , pp. 443-448
    • Baumer, A.1    Belli, S.2    Trueb, R.M.3    Schinzel, A.4
  • 9
    • 0013587987 scopus 로고
    • Congenital pilar defect showing features of pili torti
    • Beare JM (1952) Congenital pilar defect showing features of pili torti. Br J Dermatol; 64: 366-372.
    • (1952) Br J Dermatol , vol.64 , pp. 366-372
    • Beare, J.M.1
  • 10
    • 0346816584 scopus 로고    scopus 로고
    • Comel-Netherton syndrome with bacterial superinfection
    • Beljan G, Traupe H, Metze D (2003) Comel-Netherton syndrome with bacterial superinfection. Hautarzt 54: 1198-1202.
    • (2003) Hautarzt , vol.54 , pp. 1198-1202
    • Beljan, G.1    Traupe, H.2    Metze, D.3
  • 11
    • 1942517306 scopus 로고    scopus 로고
    • Giant Aplasia Cutis Congenita without Associated Anomalies
    • Benjamin LT, Trowers AB, Schachner LA (2004) Giant Aplasia Cutis Congenita without Associated Anomalies. Pediatr Dermatol 21: 150-153.
    • (2004) Pediatr Dermatol , vol.21 , pp. 150-153
    • Benjamin, L.T.1    Trowers, A.B.2    Schachner, L.A.3
  • 12
    • 0042139100 scopus 로고
    • Monilethrix and pseudomonilethri
    • Orfanos CE, Happle R (eds), Springer Berlin Heidelberg New York Tokyo
    • Bentley-Phillips B (1990) Monilethrix and Pseudomonilethrix. In: Orfanos CE, Happle R (eds) Hair and Hair diseases. Springer Berlin Heidelberg New York Tokyo, pp 423-442.
    • (1990) Hair and Hair Diseases , pp. 423-442
    • Bentley-Phillips, B.1
  • 13
    • 0030061569 scopus 로고    scopus 로고
    • Hypotrichosis, hair structure defects, hypercysteine hair and glucosuria: A new genetic syndrome?
    • Blume-Peytavi U, Fohles J, Schulz R et al (1996) Hypotrichosis, hair structure defects, hypercysteine hair and glucosuria: A new genetic syndrome? Br J Dermatol 134: 319-324.
    • (1996) Br J Dermatol , vol.134 , pp. 319-324
    • Blume-Peytavi, U.1    Fohles, J.2    Schulz, R.3
  • 14
    • 3042587795 scopus 로고    scopus 로고
    • Hair shaft abnormalities
    • Hordinsky M, Sawaya M, Scher S (eds), Churchill Livingstone Philadelphia
    • Blume-Peytavi U, Mandt N (2000), Hair shaft abnormalities. In: Hordinsky M, Sawaya M, Scher S (eds) Atlas of the Hair and Nails. Churchill Livingstone Philadelphia, pp 105-119.
    • (2000) Atlas of the Hair and Nails , pp. 105-119
    • Blume-Peytavi, U.1    Mandt, N.2
  • 16
    • 33845956647 scopus 로고    scopus 로고
    • Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: No obvious genotype-phenotype relationships
    • Botta E, Offman J, Nardo T et al (2007). Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships. Hum Mutat 28 :92-96.
    • (2007) Hum Mutat , vol.28 , pp. 92-96
    • Botta, E.1    Offman, J.2    Nardo, T.3
  • 17
    • 0003079512 scopus 로고
    • Recherches sur l'alopecie atrophiante, variete pseudopelade
    • Brocq L, Lenglet E, Ayrignac J (1905) Recherches sur l'alopecie atrophiante, variete pseudopelade. Ann Dermatol Syphilol 6:1-32.
    • (1905) Ann Dermatol Syphilol , vol.6 , pp. 1-32
    • Brocq, L.1    Lenglet, E.2    Ayrignac, J.3
  • 18
    • 0017709089 scopus 로고
    • Alopecia areata and vitiligo associated with Down's syndrome, Letter
    • Brown AC, Olkowski ZL, McLaren JR et al (1977) Alopecia areata and vitiligo associated with Down's syndrome. (Letter). Arch Derm 113: 1296.
    • (1977) Arch Derm , vol.113 , pp. 1296
    • Brown, A.C.1    Olkowski, Z.L.2    McLaren, J.R.3
  • 19
    • 0033911533 scopus 로고    scopus 로고
    • A. Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping
    • Chavanas S, Garner C, Bodemer C et al (2000) A. Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping. Am J Hum Genet 66: 914-921.
    • (2000) Am J Hum Genet , vol.66 , pp. 914-921
    • Chavanas, S.1    Garner, C.2    Bodemer, C.3
  • 20
    • 1342280466 scopus 로고    scopus 로고
    • Stratum corneum maturation. A review of neonatal skin function
    • Chiou YB, Blume-Peytavi U (2004) Stratum corneum maturation. A review of neonatal skin function. Skin Pharmacol Physiol 17: 57-66.
    • (2004) Skin Pharmacol Physiol , vol.17 , pp. 57-66
    • Chiou, Y.B.1    Blume-Peytavi, U.2
  • 21
    • 0028341036 scopus 로고
    • Pseudopelade of Brocq occurring in two brothers in childhood
    • Collier PM, James MP (1994) Pseudopelade of Brocq occurring in two brothers in childhood. Clin Exp Dermatol 19: 61-64.
    • (1994) Clin Exp Dermatol , vol.19 , pp. 61-64
    • Collier, P.M.1    James, M.P.2
  • 22
    • 0019946587 scopus 로고
    • Neurotrichosis: Hair-shaft abnormalities associated with neurological diseases
    • Coulter DL, Beals TF, Allen RJ (1982) Neurotrichosis: Hair-shaft abnormalities associated with neurological diseases. Dev Med Child Neurol; 24: 634-644.
    • (1982) Dev Med Child Neurol , vol.24 , pp. 634-644
    • Coulter, D.L.1    Beals, T.F.2    Allen, R.J.3
  • 23
    • 0015597377 scopus 로고
    • A familial syndrome of deafness, alopecia, and hypogonadism
    • Crandall BF, Samec L, Sparkes RS et al (1973) A familial syndrome of deafness, alopecia, and hypogonadism. J Pediat 82: 461-465.
    • (1973) J Pediat , vol.82 , pp. 461-465
    • Crandall, B.F.1    Samec, L.2    Sparkes, R.S.3
  • 25
    • 26444490585 scopus 로고    scopus 로고
    • Transient neonatal hair loss: A common transient neonatal dermatosis
    • Cutrone M, Grimalt R (2005) Transient neonatal hair loss: A common transient neonatal dermatosis. Eur J Pediatr 164:630-632.
    • (2005) Eur J Pediatr , vol.164 , pp. 630-632
    • Cutrone, M.1    Grimalt, R.2
  • 26
    • 0000482195 scopus 로고
    • Atrichia with papular lesions: A variant of congenital ectodermal dysplasia
    • Damste TJ, Prakken JR (1954)Atrichia with papular lesions: A variant of congenital ectodermal dysplasia. Dermatologica 108: 114-121.
    • (1954) Dermatologica , vol.108 , pp. 114-121
    • Damste, T.J.1    Prakken, J.R.2
  • 27
    • 0029742987 scopus 로고    scopus 로고
    • Clinical aspects of hair disorders
    • Dawber RPR (1996) Clinical aspects of hair disorders. Dermatol Clin 14: 753-772.
    • (1996) Dermatol Clin , vol.14 , pp. 753-772
    • Dawber, R.P.R.1
  • 28
    • 1642359198 scopus 로고    scopus 로고
    • Efficacy and tolerability of 8 weeks' treatment with terbinafine in children with tinea capitis caused by Microsporum canis: A comparison of three doses
    • Devliotou-Panagiotidou D, Koussidou-Eremondi TH (2004) Efficacy and tolerability of 8 weeks' treatment with terbinafine in children with tinea capitis caused by Microsporum canis: A comparison of three doses. J Eur Acad Dermatol Venereol 18: 155-159.
    • (2004) J Eur Acad Dermatol Venereol , vol.18 , pp. 155-159
    • Devliotou-Panagiotidou, D.1    Koussidou-Eremondi, T.H.2
  • 29
    • 3943087667 scopus 로고    scopus 로고
    • Severe monilethrix associated with intractable scalp pruritus, posterior subcapsular cataract, brachiocephaly, and distinct facial features: A new variant of monilethrix syndrome?
    • Erbagci Z, Erbagci I, Erbagci H et al (2004) Severe monilethrix associated with intractable scalp pruritus, posterior subcapsular cataract, brachiocephaly, and distinct facial features: A new variant of monilethrix syndrome? Pediatr Dermatol. 21 :486-490.
    • (2004) Pediatr Dermatol , vol.21 , pp. 486-490
    • Erbagci, Z.1    Erbagci, I.2    Erbagci, H.3
  • 31
    • 0041868060 scopus 로고    scopus 로고
    • Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-Affected skin from C3H/HeJ mice
    • Freyschmidt-Paul P, McElwee KJ, Botchkarev V et al (2003) Fas-deficient C3.MRL-Tnfrsf6(lpr) mice and Fas ligand-deficient C3H/HeJ-Tnfsf6(gld) mice are relatively resistant to the induction of alopecia areata by grafting of alopecia areata-Affected skin from C3H/HeJ mice. J Investig Dermatol Symp Proc 8: 104-108.
    • (2003) J Investig Dermatol Symp Proc , vol.8 , pp. 104-108
    • Freyschmidt-Paul, P.1    McElwee, K.J.2    Botchkarev, V.3
  • 32
    • 0029098087 scopus 로고
    • Tumor necrosis factor alpha (TNF-Alpha) gene polymorphism in alopecia areata
    • Galbraith GMP, Pandey JP (1995) Tumor necrosis factor alpha (TNF-Alpha) gene polymorphism in alopecia areata. Hum Genet 96: 433-436.
    • (1995) Hum Genet , vol.96 , pp. 433-436
    • Galbraith, G.M.P.1    Pandey, J.P.2
  • 35
    • 33748128064 scopus 로고    scopus 로고
    • Brachial artery aneurysms in Menkes disease
    • Godwin SC, Shawker T, Chang B et al (2006) Brachial artery aneurysms in Menkes disease. J Pediatr 149: 412-415.
    • (2006) J Pediatr , vol.149 , pp. 412-415
    • Godwin, S.C.1    Shawker, T.2    Chang, B.3
  • 36
    • 84892288711 scopus 로고
    • Narbige alopezien
    • Orfanos CE (ed), 2nd Edition. Fischer Verlag Stuttgart
    • Goerz G, Kind R (1991) Narbige Alopezien. In: Orfanos CE (ed) Haar und Haarkrankheiten. 2nd Edition. Fischer Verlag Stuttgart pp 605-637.
    • (1991) Haar Und Haarkrankheiten , pp. 605-637
    • Goerz, G.1    Kind, R.2
  • 37
    • 33644835049 scopus 로고    scopus 로고
    • Keratosis follicularis spinulosa decalvans and acne keloidalis nuchae
    • Goh MS, Magee J, Chong AH (2005) Keratosis follicularis spinulosa decalvans and acne keloidalis nuchae. Australas J Dermatol 46:257-260.
    • (2005) Australas J Dermatol , vol.46 , pp. 257-260
    • Goh, M.S.1    Magee, J.2    Chong, A.H.3
  • 38
    • 19944380178 scopus 로고    scopus 로고
    • A survey of Japanese patients with Menkes disease from 1990 to 2003: Incidence and early signs before typical symptomatic onset, pointing the way to earlier diagnosis
    • Gu YH, Kodama H, Shiga K et al (2005) A survey of Japanese patients with Menkes disease from 1990 to 2003: incidence and early signs before typical symptomatic onset, pointing the way to earlier diagnosis. J Inherit Metab Dis. 28:473-478.
    • (2005) J Inherit Metab Dis , vol.28 , pp. 473-478
    • Gu, Y.H.1    Kodama, H.2    Shiga, K.3
  • 39
    • 0024533023 scopus 로고
    • Loose anagen hair of childhood: The phenomenon of easily pluckable hair
    • Hamm H, Traup, H (1989) Loose anagen hair of childhood: The phenomenon of easily pluckable hair. J Am Acad Derm 20: 242-248.
    • (1989) J Am Acad Derm , vol.20 , pp. 242-248
    • Hamm, H.1    Traup, H.2
  • 40
    • 0037259065 scopus 로고    scopus 로고
    • Traction alopecia in children
    • Hantash BM, Schwartz RA (2003) Traction alopecia in children. Cutis 71: 18-20.
    • (2003) Cutis , vol.71 , pp. 18-20
    • Hantash, B.M.1    Schwartz, R.A.2
  • 41
    • 0041659268 scopus 로고    scopus 로고
    • Congenital triangular alopecia may be categorized as a paradominant trait
    • Happle R (2003) Congenital triangular alopecia may be categorized as a paradominant trait. Eur J Dermatol 13: 346-347.
    • (2003) Eur J Dermatol , vol.13 , pp. 346-347
    • Happle, R.1
  • 42
    • 0021740146 scopus 로고
    • 1.25-dihydroxyvitamin D resistance, rickets, and alopecia
    • Hochberg Z, Benderli A, Levy J et al (1984) 1.25-dihydroxyvitamin D resistance, rickets, and alopecia. Am J Med 77: 805-811.
    • (1984) Am J Med , vol.77 , pp. 805-811
    • Hochberg, Z.1    Benderli, A.2    Levy, J.3
  • 43
    • 0018864378 scopus 로고
    • Regional development of the human epidermis in the first trimester embryo and the second trimester fetus (ages related to the timing of amniocentesis and fetal biopsy)
    • 1980
    • Holbrook KA, Odland GF(1980) Regional development of the human epidermis in the first trimester embryo and the second trimester fetus (ages related to the timing of amniocentesis and fetal biopsy). J Invest Dermatol 1980 74: 161-168.
    • (1980) J Invest Dermatol , vol.74 , pp. 161-168
    • Holbrook, K.A.1    Odland, G.F.2
  • 44
    • 22944457279 scopus 로고    scopus 로고
    • Olsen EA ed., 2nd edn. McGraw-Hill Medical Publishing Division, New York Chicago San Francisco
    • Hordinsky MK, Alopecia areata. In: Olsen EA ed. (2003) Disorders of hair growth. 2nd edn. McGraw-Hill Medical Publishing Division, New York Chicago San Francisco, p 239.
    • (2003) Disorders of Hair Growth , pp. 239
    • Hordinsky, M.K.1    Alopecia, A.2
  • 46
    • 0035010089 scopus 로고    scopus 로고
    • Trichothiodystrophy: Update on the sulfur-deficient brittle hair syndromes
    • Itin PH, Sarasin A, Pittelkow MR (2001) Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes. J Am Acad Dermatol 44: 891-920.
    • (2001) J Am Acad Dermatol , vol.44 , pp. 891-920
    • Itin, P.H.1    Sarasin, A.2    Pittelkow, M.R.3
  • 48
    • 16844372411 scopus 로고    scopus 로고
    • Apparent fragility of African hair is unrelated to the cystine-rich protein distribution: A cytochemical electron microscopic study
    • Khumalo NP, Dawber RP, Ferguson DJ (2005) Apparent fragility of African hair is unrelated to the cystine-rich protein distribution: A cytochemical electron microscopic study. Exp Dermatol. 14:311-314.
    • (2005) Exp Dermatol , vol.14 , pp. 311-314
    • Khumalo, N.P.1    Dawber, R.P.2    Ferguson, D.J.3
  • 49
    • 0021285323 scopus 로고
    • Trichothiodystrophy- neurotrichocutaneous syndrome of Pollitt: A report of two unrelated cases
    • King MD, Gummer CL, Stephenson JBP (1984) Trichothiodystrophy- neurotrichocutaneous syndrome of Pollitt: A report of two unrelated cases. J Med Genet 21: 286-289.
    • (1984) J Med Genet , vol.21 , pp. 286-289
    • King, M.D.1    Gummer, C.L.2    Stephenson, J.B.P.3
  • 50
    • 0012920802 scopus 로고    scopus 로고
    • Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: Implications for protein structure and clinical phenotype
    • Korge BP, Hamm H, Jury CS (1999) Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype. J Invest Dermatol 113: 607-612.
    • (1999) J Invest Dermatol , vol.113 , pp. 607-612
    • Korge, B.P.1    Hamm, H.2    Jury, C.S.3
  • 51
    • 0038722047 scopus 로고    scopus 로고
    • Towards a new classification of ectodermal dysplasias
    • Lamartine J (2003) Towards a new classification of ectodermal dysplasias. Clin Exp Dermatol 28: 351-355.
    • (2003) Clin Exp Dermatol , vol.28 , pp. 351-355
    • Lamartine, J.1
  • 52
    • 58149211753 scopus 로고
    • Approach to dermatologic disorders in black children
    • Laude TA (1995) Approach to dermatologic disorders in black children. Semin Dermatol 14:15-20.
    • (1995) Semin Dermatol , vol.14 , pp. 15-20
    • Laude, T.A.1
  • 53
    • 0034074163 scopus 로고    scopus 로고
    • A. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis
    • Lefevre P, Rochat A, Bodemer C et al (2000) A. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis. Eur J Hum Genet 8: 273-279.
    • (2000) Eur J Hum Genet , vol.8 , pp. 273-279
    • Lefevre, P.1    Rochat, A.2    Bodemer, C.3
  • 54
    • 33748763831 scopus 로고    scopus 로고
    • Structural and molecular hair abnormalities in trichothiodystrophy
    • Liang C, Morris A, Schlucker S et al (2006) Structural and molecular hair abnormalities in trichothiodystrophy. J Invest Dermatol 126:2210-2216.
    • (2006) J Invest Dermatol , vol.126 , pp. 2210-2216
    • Liang, C.1    Morris, A.2    Schlucker, S.3
  • 55
    • 0029886612 scopus 로고    scopus 로고
    • Trichorrhexis nodosa: A manifestation of hypothyroidism
    • Lurie R, Hodak E, Ginzburg A et al (1996) Trichorrhexis nodosa: A manifestation of hypothyroidism. Cutis. 57:358-359.
    • (1996) Cutis , vol.57 , pp. 358-359
    • Lurie, R.1    Hodak, E.2    Ginzburg, A.3
  • 56
    • 3042597925 scopus 로고    scopus 로고
    • Differential diagnosis of hair loss in children
    • Mandt N. Vogt A, Blume-Peytavi U (2004) Differential diagnosis of hair loss in children. J Dtsch Dermatol Ges 2:399-411.
    • (2004) J Dtsch Dermatol Ges , vol.2 , pp. 399-411
    • Mandt, N.V.A.1    Blume-Peytavi, U.2
  • 57
    • 0022501061 scopus 로고
    • Analysis of the relation between alopecia and resistance to 1.25-dihydroxyvitamin D
    • Marx SJ, Bliziotes MM, Nanes M (1986) Analysis of the relation between alopecia and resistance to 1.25-dihydroxyvitamin D. Clin Endocrinol 25: 373-381.
    • (1986) Clin Endocrinol , vol.25 , pp. 373-381
    • Marx, S.J.1    Bliziotes, M.M.2    Nanes, M.3
  • 59
    • 0023898471 scopus 로고
    • Kinky hair disease: Twenty five years later
    • Menkes JH (1988) Kinky hair disease: Twenty five years later. Brain Dev 10: 77-79.
    • (1988) Brain Dev , vol.10 , pp. 77-79
    • Menkes, J.H.1
  • 60
    • 0034800098 scopus 로고    scopus 로고
    • Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene
    • Miller J, Djabali K, Chen T et al (2001) Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene. J Invest Dermatol 117: 612-617.
    • (2001) J Invest Dermatol , vol.117 , pp. 612-617
    • Miller, J.1    Djabali, K.2    Chen, T.3
  • 61
    • 0022338262 scopus 로고
    • Ectodermal manifestations in Menkes disease
    • Moore C M.; Howell R (1985) Ectodermal manifestations in Menkes disease. Clin. Genet 28: 532-540.
    • (1985) Clin. Genet , vol.28 , pp. 532-540
    • Moore, C.M.1    Howell, R.2
  • 62
    • 0036277966 scopus 로고    scopus 로고
    • Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing
    • Muller FB, Hausser I, Berg D et al (2002) Genetic analysis of a severe case of Netherton syndrome and application for prenatal testing. Br J Dermatol 146: 495-499.
    • (2002) Br J Dermatol , vol.146 , pp. 495-499
    • Muller, F.B.1    Hausser, I.2    Berg, D.3
  • 63
    • 0036932078 scopus 로고    scopus 로고
    • Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome
    • Nassogne MC, Sharrard M, Hertz-Pannier L et al (2002) Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome. Childs Nerv Syst 18: 729-731.
    • (2002) Childs Nerv Syst , vol.18 , pp. 729-731
    • Nassogne, M.C.1    Sharrard, M.2    Hertz-Pannier, L.3
  • 64
    • 17344370417 scopus 로고    scopus 로고
    • A gene for universal congenital alopecia maps to chromosome 8p21-22
    • Nothen MM, Cichon S, Vogt IR et al (1998) A gene for universal congenital alopecia maps to chromosome 8p21-22. Am J Hum Genet 62: 386-390.
    • (1998) Am J Hum Genet , vol.62 , pp. 386-390
    • Nothen, M.M.1    Cichon, S.2    Vogt, I.R.3
  • 65
    • 3042587794 scopus 로고    scopus 로고
    • Hair disorders
    • Harper J, Oranje A, Prose N (eds), Blackwell Science Oxford
    • Olsen EA (2000) Hair disorders. In: Harper J, Oranje A, Prose N (eds) Textbook of pediatric dermatology. Blackwell Science Oxford, pp 1463-1490.
    • (2000) Textbook of Pediatric Dermatology , pp. 1463-1490
    • Olsen, E.A.1
  • 67
    • 0028127041 scopus 로고
    • Ectodermal dysplasias: A clinical classification and a causal review
    • Pinheiro M, Freire-Maia N (1994) Ectodermal dysplasias: A clinical classification and a causal review. Am J Med Genet 53: 153-162.
    • (1994) Am J Med Genet , vol.53 , pp. 153-162
    • Pinheiro, M.1    Freire-Maia, N.2
  • 68
    • 0036907094 scopus 로고    scopus 로고
    • Tinea capitis: Epidemiology, diagnosis and management strategies
    • Pomeranz AJ, Sabnis SS (2002) Tinea capitis: Epidemiology, diagnosis and management strategies. Paediatr Drugs 4: 779-783.
    • (2002) Paediatr Drugs , vol.4 , pp. 779-783
    • Pomeranz, A.J.1    Sabnis, S.S.2
  • 69
    • 0031968339 scopus 로고    scopus 로고
    • Keratosis follicularis spinulosa decalvans: Confirmation of linkage to Xp22.13-p22.2
    • Porteous ME, Strain L, Logie LJ et al (1998) Keratosis follicularis spinulosa decalvans: confirmation of linkage to Xp22.13-p22.2. J Med Genet 35: 336-337.
    • (1998) J Med Genet , vol.35 , pp. 336-337
    • Porteous, M.E.1    Strain, L.2    Logie, L.J.3
  • 70
    • 8944248842 scopus 로고
    • Strukturanomalien des Haarschaftes
    • Orfanos CE (ed), 2nd Edition. Fischer Verlag Stuttgart
    • Price VH (1991) Strukturanomalien des Haarschaftes. In: Orfanos CE (ed) Haar und Haarkrankheiten. 2nd Edition. Fischer Verlag Stuttgart pp 387 - 446.
    • (1991) Haar Und Haarkrankheiten , pp. 387-446
    • Price, V.H.1
  • 71
    • 0037805219 scopus 로고    scopus 로고
    • Androgenetic alopecia in adolescents
    • Price VH (2003) Androgenetic alopecia in adolescents. Cutis 71: 115-121.
    • (2003) Cutis , vol.71 , pp. 115-121
    • Price, V.H.1
  • 73
    • 0019245621 scopus 로고
    • Trichothiodystrophy: Sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex
    • Price VH, Odom RB, Ward WH et al (1980) Trichothiodystrophy: Sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex. Arch Derm 116: 1375-1384.
    • (1980) Arch Derm , vol.116 , pp. 1375-1384
    • Price, V.H.1    Odom, R.B.2    Ward, W.H.3
  • 74
    • 0034535697 scopus 로고    scopus 로고
    • Ectodermal dysplasias: Not only 'skin' deep
    • Priolo M, Silengo M, Lerone M et al (2000) Ectodermal dysplasias: not only 'skin' deep. Clin Genet 58: 415-430.
    • (2000) Clin Genet , vol.58 , pp. 415-430
    • Priolo, M.1    Silengo, M.2    Lerone, M.3
  • 75
    • 0034052447 scopus 로고    scopus 로고
    • In utero diagnosis of trichothiodystrophy by endoscopically- guided fetal eyebrow biopsy
    • Quintero RA, Morales WJ, Gilbert-Barness E et al (2000) In utero diagnosis of trichothiodystrophy by endoscopically- guided fetal eyebrow biopsy. Fetal Diagn Ther 15:152-155.
    • (2000) Fetal Diagn Ther , vol.15 , pp. 152-155
    • Quintero, R.A.1    Morales, W.J.2    Gilbert-Barness, E.3
  • 76
    • 0020700243 scopus 로고
    • Keratosis follicularis spinulosa decalvans. Report of two cases and literature review
    • Rand R, Baden HP (1983). Keratosis follicularis spinulosa decalvans. Report of two cases and literature review. Arch Dermatol 119: 22-26.
    • (1983) Arch Dermatol , vol.119 , pp. 22-26
    • Rand, R.1    Baden, H.P.2
  • 77
    • 22944472454 scopus 로고    scopus 로고
    • Infectious, physical, and inflammatory causes of hair and scalp abnormalities
    • Olsen EA ed., 2nd edn. McGraw-Hill Medical Publishing Division, New York Chicago San Francisco p
    • Roberts JL, De Villez RL, Infectious, physical, and inflammatory causes of hair and scalp abnormalities. In: In: Olsen EA ed. (2003) Disorders of hair growth. 2nd edn. McGraw-Hill Medical Publishing Division, New York Chicago San Francisco p 87.
    • (2003) Disorders of Hair Growth , vol.87
    • Roberts, J.L.1    De Villez, R.L.2
  • 78
    • 33749684977 scopus 로고    scopus 로고
    • Videodermoscopy in the evaluation of hair and scalp disorders
    • Ross EK, Vincenzi C, Tosti A (2006) Videodermoscopy in the evaluation of hair and scalp disorders. J Am Acad Dermatol 55:799-806.
    • (2006) J Am Acad Dermatol , vol.55 , pp. 799-806
    • Ross, E.K.1    Vincenzi, C.2    Tosti, A.3
  • 79
    • 0026664103 scopus 로고
    • Prevalence of alopecia areata in the First National Health and Nutrition Examination Survey, Letter
    • Safavi K (1992) Prevalence of alopecia areata in the First National Health and Nutrition Examination Survey. (Letter). Arch Derm 128: 702.
    • (1992) Arch Derm , vol.128 , pp. 702
    • Safavi, K.1
  • 80
    • 0013587986 scopus 로고
    • Pili moniliformis
    • Berl
    • Schutz J (1900) Pili moniliformis. Arch Derm Syph (Berl) 53: 69.
    • (1900) Arch Derm Syph , vol.53 , pp. 69
    • Schutz, J.1
  • 82
    • 33750044566 scopus 로고    scopus 로고
    • Low but detectable serum levels of tacrolimus seen with the use of very dilute, extemporaneously compounded formulations of tacrolimus ointment in the treatment of patients with netherton syndrome
    • Shah KN, Yan AC (2006) Low but detectable serum levels of tacrolimus seen with the use of very dilute, extemporaneously compounded formulations of tacrolimus ointment in the treatment of patients with netherton syndrome. Arch Dermatol 142:1362-1363.
    • (2006) Arch Dermatol , vol.142 , pp. 1362-1363
    • Shah, K.N.1    Yan, A.C.2
  • 83
    • 33745569010 scopus 로고    scopus 로고
    • Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis
    • Shimomura Y, Sakamoto F, Kariya N et al (2006) Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis. J Invest Dermatol. 126:1281-1285.
    • (2006) J Invest Dermatol , vol.126 , pp. 1281-1285
    • Shimomura, Y.1    Sakamoto, F.2    Kariya, N.3
  • 84
    • 0344104550 scopus 로고
    • Ueber einen in der menschlichen Pathologie noch nicht beobachteten Vererbungsmodus: Dominant geschlechtsgebundene Vererbung
    • Siemens HW (1925) Ueber einen in der menschlichen Pathologie noch nicht beobachteten Vererbungsmodus: dominant geschlechtsgebundene Vererbung. Arch Rass Ges Biol 17:47-61.
    • (1925) Arch Rass Ges Biol , vol.17 , pp. 47-61
    • Siemens, H.W.1
  • 86
    • 0007442140 scopus 로고
    • Traction alopecia
    • Slepyan AH (1958) Traction alopecia. AMA Arch Derm 78:395-398.
    • (1958) AMA Arch Derm , vol.78 , pp. 395-398
    • Slepyan, A.H.1
  • 87
    • 0026468040 scopus 로고
    • Clinical response of alopecia, trichorrhexis nodosa, and dry, scaly skin to zinc supplementation
    • Slonim AE, Sadick N, Pugliese M et al (1992) Clinical response of alopecia, trichorrhexis nodosa, and dry, scaly skin to zinc supplementation. J Pediatr 121:890-895.
    • (1992) J Pediatr , vol.121 , pp. 890-895
    • Slonim, A.E.1    Sadick, N.2    Pugliese, M.3
  • 88
    • 0028893542 scopus 로고
    • Netherton's syndrome. A syndrome of elevated IgE and characteristic skin and hair findings
    • Smith DL, Smith JG, Wong SW et al (1995) Netherton's syndrome. a syndrome of elevated IgE and characteristic skin and hair findings. J Allergy Clin Immunol 95: 116-123.
    • (1995) J Allergy Clin Immunol , vol.95 , pp. 116-123
    • Smith, D.L.1    Smith, J.G.2    Wong, S.W.3
  • 89
    • 0030010193 scopus 로고    scopus 로고
    • Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13
    • Stevens HP, Kelsell DP, Bryant SP et al (1996) Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13. J Invest Dermatol 106: 795-797.
    • (1996) J Invest Dermatol , vol.106 , pp. 795-797
    • Stevens, H.P.1    Kelsell, D.P.2    Bryant, S.P.3
  • 90
    • 0037960261 scopus 로고    scopus 로고
    • Major locus on mouse chromosome 17 and minor locus on chromosome 9 are linked with alopecia areata in C3H/HeJ mice
    • Sundberg JP, Boggess D, Silva KA (2003) Major locus on mouse chromosome 17 and minor locus on chromosome 9 are linked with alopecia areata in C3H/HeJ mice. J Invest Dermatol 120: 771-775.
    • (2003) J Invest Dermatol , vol.120 , pp. 771-775
    • Sundberg, J.P.1    Boggess, D.2    Silva, K.A.3
  • 92
    • 0347003662 scopus 로고    scopus 로고
    • Primary cicatricial alopecias: Clinicopathology of 112 cases
    • Tan E, Martinka M, Ball N et al (2004) Primary cicatricial alopecias: clinicopathology of 112 cases. J Am Acad Dermatol 50: 25-32.
    • (2004) J Am Acad Dermatol , vol.50 , pp. 25-32
    • Tan, E.1    Martinka, M.2    Ball, N.3
  • 93
    • 0015087003 scopus 로고
    • Ichthyosiform erythroderma, hair shaft abnormalities, and mental and growth retardation: A new recessive disorder
    • Tay CH (1971) Ichthyosiform erythroderma, hair shaft abnormalities, and mental and growth retardation: A new recessive disorder. Arch Derm 104: 4-13.
    • (1971) Arch Derm , vol.104 , pp. 4-13
    • Tay, C.H.1
  • 95
    • 0016337743 scopus 로고
    • Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance
    • Toribio J, Quinones PA (1974) Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance. Br J Dermatol 91: 687-696.
    • (1974) Br J Dermatol , vol.91 , pp. 687-696
    • Toribio, J.1    Quinones, P.A.2
  • 96
    • 0036216383 scopus 로고    scopus 로고
    • Loose anagen hair syndrome and loose anagen hair
    • Tosti A, Piraccini BM (2002) Loose anagen hair syndrome and loose anagen hair. Arch Dermatol 138:521-522.
    • (2002) Arch Dermatol , vol.138 , pp. 521-522
    • Tosti, A.1    Piraccini, B.M.2
  • 97
    • 0029685249 scopus 로고    scopus 로고
    • Early copper-histidine treatment for Menkes disease
    • Tumer Z, Horn N, Tonnesen T (1996) Early copper-histidine treatment for Menkes disease. Nat Genet 12: 11-13.
    • (1996) Nat Genet , vol.12 , pp. 11-13
    • Tumer, Z.1    Horn, N.2    Tonnesen, T.3
  • 98
    • 0026518090 scopus 로고
    • Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2
    • Tumer Z, Tommerup N, Tonnesen T et al (1992) Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2. Hum Genet 88: 668-672.
    • (1992) Hum Genet , vol.88 , pp. 668-672
    • Tumer, Z.1    Tommerup, N.2    Tonnesen, T.3
  • 99
    • 0031595379 scopus 로고    scopus 로고
    • Bjornstad syndrome in a patient with mental retardation
    • Van Buggenhout G, Trommelen J, Hamel B (1998) Bjornstad syndrome in a patient with mental retardation. Genet Counsel 9: 201-204.
    • (1998) Genet Counsel , vol.9 , pp. 201-204
    • Van Buggenhout, G.1    Trommelen, J.2    Hamel, B.3
  • 100
    • 0026725963 scopus 로고
    • The genetic risk for alopecia areata in first degree relatives of severely affected patients. An estimate
    • Van der Steen P, Traupe H, Happle R et al (1992) The genetic risk for alopecia areata in first degree relatives of severely affected patients. An estimate. Acta Derm Venereol 72: 373-375.
    • (1992) Acta Derm Venereol , vol.72 , pp. 373-375
    • Van Der Steen, P.1    Traupe, H.2    Happle, R.3
  • 101
    • 33746113338 scopus 로고    scopus 로고
    • Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
    • Wali A, Ansar M, Khan MN, Ahmad W (2006) Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene. Clin Exp Dermatol 31:695-698.
    • (2006) Clin Exp Dermatol , vol.31 , pp. 695-698
    • Wali, A.1    Ansar, M.2    Khan, M.N.3    Ahmad, W.4
  • 102
    • 0034753856 scopus 로고    scopus 로고
    • Trichotillomania. Presentation, etiology, diagnosis and therapy
    • Walsh KH, McDougle CJ (2001) Trichotillomania. Presentation, etiology, diagnosis and therapy. Am J Clin Dermatol 2: 327-333.
    • (2001) Am J Clin Dermatol , vol.2 , pp. 327-333
    • Walsh, K.H.1    McDougle, C.J.2
  • 103
    • 0026091813 scopus 로고
    • The management of traumatic scalp injuries: Report of cases
    • Welch TB, Boyne PJ (1991) The management of traumatic scalp injuries: Report of cases. J Oral Maxillofac Surg 49: 1007-1014.
    • (1991) J Oral Maxillofac Surg , vol.49 , pp. 1007-1014
    • Welch, T.B.1    Boyne, P.J.2
  • 104
    • 0024673424 scopus 로고
    • Localized trichorrhexis nodosa
    • Whiting DA (1989) Localized trichorrhexis nodosa.J Am Acad Dermatol 20: 854.
    • (1989) J Am Acad Dermatol , vol.20 , pp. 854
    • Whiting, D.A.1
  • 105
    • 0033010956 scopus 로고    scopus 로고
    • Traumatic alopecia
    • Whiting DA (1999) Traumatic alopecia. Int J Dermatol 38 Suppl 1: 34-44.
    • (1999) Int J Dermatol , vol.1 , Issue.38 SUPPL. , pp. 34-44
    • Whiting, D.A.1
  • 107
    • 0036175776 scopus 로고    scopus 로고
    • Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype
    • Wolf B (2002) Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype. Eur J Pediatr 161: 167-168.
    • (2002) Eur J Pediatr , vol.161 , pp. 167-168
    • Wolf, B.1


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