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Volumn 29, Issue 2, 2011, Pages 205-225

Blaschko lines and other patterns of cutaneous mosaicism

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOME MOSAICISM; BLASCHKO LINE; CUTANEOUS MOSAICISM; DIFFERENTIAL DIAGNOSIS; DOMINANT INHERITANCE; EPIGENETICS; GENE MUTATION; HUMAN; HYPERPIGMENTATION; HYPOPIGMENTATION; PRIORITY JOURNAL; SEX CHROMOSOME MOSAICISM; SKIN EXAMINATION; SKIN MANIFESTATION; X CHROMOSOME LINKED DISORDER;

EID: 79952396239     PISSN: 0738081X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clindermatol.2010.09.012     Document Type: Article
Times cited : (84)

References (82)
  • 2
    • 0035088609 scopus 로고    scopus 로고
    • The lines of Blaschko on the head and neck
    • Happle R., Assim A. The lines of Blaschko on the head and neck. J Am Acad Dermatol 2001, 44:612-615.
    • (2001) J Am Acad Dermatol , vol.44 , pp. 612-615
    • Happle, R.1    Assim, A.2
  • 3
    • 0017644223 scopus 로고
    • Genetische Bedeutung der Blaschoschen Linien
    • Happle R. Genetische Bedeutung der Blaschoschen Linien. Z Hautkr 1977, 52:935-944.
    • (1977) Z Hautkr , vol.52 , pp. 935-944
    • Happle, R.1
  • 4
    • 0027452134 scopus 로고
    • Mosaicism in human skin: Understanding the pattern and mechanisms
    • Happle R. Mosaicism in human skin: Understanding the pattern and mechanisms. Arch Dermatol 1993, 129:1460-1470.
    • (1993) Arch Dermatol , vol.129 , pp. 1460-1470
    • Happle, R.1
  • 5
    • 0033535478 scopus 로고    scopus 로고
    • X-chromosome inactivation
    • Lyon M.F. X-chromosome inactivation. Curr Biol 1999, 9:235-237.
    • (1999) Curr Biol , vol.9 , pp. 235-237
    • Lyon, M.F.1
  • 6
    • 57349094375 scopus 로고    scopus 로고
    • X-chromosome inactivation and skin disease
    • Sun B.K., Tsao H. X-chromosome inactivation and skin disease. J Invest Dermatol 2008, 128:2753-2759.
    • (2008) J Invest Dermatol , vol.128 , pp. 2753-2759
    • Sun, B.K.1    Tsao, H.2
  • 7
    • 15244353967 scopus 로고    scopus 로고
    • X-inactivation profile reveals extensive variability in X-linked gene expression in females
    • Carrel L., Willard H.F. X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature 2005, 434:400-404.
    • (2005) Nature , vol.434 , pp. 400-404
    • Carrel, L.1    Willard, H.F.2
  • 8
    • 70349318211 scopus 로고    scopus 로고
    • The impact of retrotransposons on human genome evolution
    • Cordaux R., Batzer M.A. The impact of retrotransposons on human genome evolution. Nat Rev Genet 2009, 10:691-703.
    • (2009) Nat Rev Genet , vol.10 , pp. 691-703
    • Cordaux, R.1    Batzer, M.A.2
  • 9
    • 0035065510 scopus 로고    scopus 로고
    • Retrotransposons as epigenetic mediators of phenotypic variation in mammals
    • Whitelaw E., Martin D.I.K. Retrotransposons as epigenetic mediators of phenotypic variation in mammals. Nat Genet 2001, 27:361-364.
    • (2001) Nat Genet , vol.27 , pp. 361-364
    • Whitelaw, E.1    Martin, D.I.K.2
  • 10
    • 70349499475 scopus 로고    scopus 로고
    • Monoallelic expression on autosomes may explain an unusual heritable form of pigmentary mosaicism: a historical case revisited
    • Happle R. Monoallelic expression on autosomes may explain an unusual heritable form of pigmentary mosaicism: a historical case revisited. Clin Exp Dermatol 2009, 34:834-837.
    • (2009) Clin Exp Dermatol , vol.34 , pp. 834-837
    • Happle, R.1
  • 11
    • 0036835316 scopus 로고    scopus 로고
    • New aspects of cutaneous mosaicism. Dohi memorial lecture
    • Happle R. New aspects of cutaneous mosaicism. Dohi memorial lecture. J Dermatol 2002, 29:681-692.
    • (2002) J Dermatol , vol.29 , pp. 681-692
    • Happle, R.1
  • 12
    • 79952420758 scopus 로고    scopus 로고
    • Cytogenetic and molecular evidence for cutaneous mosaicism: the ectodermal origin of Blaschko lines
    • Moss C. Cytogenetic and molecular evidence for cutaneous mosaicism: the ectodermal origin of Blaschko lines. Am J Med Genet 1999, 331:1408-1415.
    • (1999) Am J Med Genet , vol.331 , pp. 1408-1415
    • Moss, C.1
  • 13
    • 15244349724 scopus 로고    scopus 로고
    • Piecing together the puzzle of cutaneous mosaicism
    • Paller A.S. Piecing together the puzzle of cutaneous mosaicism. J Clin Invest 2004, 114:1407-1409.
    • (2004) J Clin Invest , vol.114 , pp. 1407-1409
    • Paller, A.S.1
  • 14
    • 0027171215 scopus 로고
    • Epidermal mosaicism and Blaschko's lines
    • Moss C., Larkins S., Stacey M., et al. Epidermal mosaicism and Blaschko's lines. J Med Genet 1993, 30:752-755.
    • (1993) J Med Genet , vol.30 , pp. 752-755
    • Moss, C.1    Larkins, S.2    Stacey, M.3
  • 15
    • 0028135470 scopus 로고
    • Genetic and clinical mosaicism in a type of epidermal nevus
    • Paller A.S., Syder A.J., Chan Y.M., et al. Genetic and clinical mosaicism in a type of epidermal nevus. N Engl J Med 1994, 1408-1415.
    • (1994) N Engl J Med , pp. 1408-1415
    • Paller, A.S.1    Syder, A.J.2    Chan, Y.M.3
  • 16
    • 70349511050 scopus 로고    scopus 로고
    • Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes
    • Taibjee S.M., Hall D., Balderson D., et al. Keratinocyte cytogenetics in 10 patients with pigmentary mosaicism: identification of one case of trisomy 20 mosaicism confined to keratinocytes. Clin Exp Dermatol 2009, 34:823-829.
    • (2009) Clin Exp Dermatol , vol.34 , pp. 823-829
    • Taibjee, S.M.1    Hall, D.2    Balderson, D.3
  • 17
    • 0027200119 scopus 로고
    • Pigmentary patterns associated with human mosaicism: a proposed classification
    • Happle R. Pigmentary patterns associated with human mosaicism: a proposed classification. Eur J Dermatol 1993, 3:170-174.
    • (1993) Eur J Dermatol , vol.3 , pp. 170-174
    • Happle, R.1
  • 18
    • 0028336004 scopus 로고
    • Melanotic macules following Blaschko's lines in McCune-Albright syndrome
    • Rieger E., Kofler R., Borkenstein M., et al. Melanotic macules following Blaschko's lines in McCune-Albright syndrome. Br J Dermatol 1994, 130:215-220.
    • (1994) Br J Dermatol , vol.130 , pp. 215-220
    • Rieger, E.1    Kofler, R.2    Borkenstein, M.3
  • 19
    • 2442473829 scopus 로고    scopus 로고
    • Activating Gs alpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome-a European Collaborative Study
    • Lumbroso S., Paris F., Sultan C. Activating Gs alpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome-a European Collaborative Study. J Clin Endocrinol Metab 2004, 89:2107-2113.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 2107-2113
    • Lumbroso, S.1    Paris, F.2    Sultan, C.3
  • 20
    • 28344436466 scopus 로고    scopus 로고
    • Delineation of the various shapes and patterns of nevi
    • Torrelo A., Baselga E., Nagore E., et al. Delineation of the various shapes and patterns of nevi. Eur J Dermatol 2005, 15:439-450.
    • (2005) Eur J Dermatol , vol.15 , pp. 439-450
    • Torrelo, A.1    Baselga, E.2    Nagore, E.3
  • 21
    • 0019130148 scopus 로고
    • Pigment anomalies of the skin in human chimaera: their relation to systematized naevi
    • Findlay G.H., Moores P.P. Pigment anomalies of the skin in human chimaera: their relation to systematized naevi. Br J Dermatol 1980, 103:489-498.
    • (1980) Br J Dermatol , vol.103 , pp. 489-498
    • Findlay, G.H.1    Moores, P.P.2
  • 22
    • 41149139492 scopus 로고    scopus 로고
    • Between light and dark, the chimera comes out
    • Lipsker D., Flory E., Wiesel M.L., et al. Between light and dark, the chimera comes out. Arch Dermatol 2008, 144:327-330.
    • (2008) Arch Dermatol , vol.144 , pp. 327-330
    • Lipsker, D.1    Flory, E.2    Wiesel, M.L.3
  • 23
    • 0035130253 scopus 로고    scopus 로고
    • Phylloid hypomelanosis and mosaic trisomy 13: a new etiologically defined neurocutaneous syndrome
    • Happle R. Phylloid hypomelanosis and mosaic trisomy 13: a new etiologically defined neurocutaneous syndrome. Hautarzt 2001, 52:3-5.
    • (2001) Hautarzt , vol.52 , pp. 3-5
    • Happle, R.1
  • 24
    • 66149086851 scopus 로고    scopus 로고
    • Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity
    • Gonzalez-Ensenat M.A., Vicente A., Poo P., et al. Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entity. Arch Dermatol 2009, 145:576-578.
    • (2009) Arch Dermatol , vol.145 , pp. 576-578
    • Gonzalez-Ensenat, M.A.1    Vicente, A.2    Poo, P.3
  • 25
    • 0041411160 scopus 로고    scopus 로고
    • Pigmentary mosaicism with mosaic chromosome 5p tetrasomy
    • Hansen L.K., Brandrup F., Rasmussen K. Pigmentary mosaicism with mosaic chromosome 5p tetrasomy. Br J Dermatol 2003, 149:414-416.
    • (2003) Br J Dermatol , vol.149 , pp. 414-416
    • Hansen, L.K.1    Brandrup, F.2    Rasmussen, K.3
  • 26
    • 61849107312 scopus 로고    scopus 로고
    • A case of hypermelanosis in a phylloid pattern
    • Hwang S.W., Cho K.J., Kang J.H., et al. A case of hypermelanosis in a phylloid pattern. J Am Acad Dermatol 2009, 60:697-700.
    • (2009) J Am Acad Dermatol , vol.60 , pp. 697-700
    • Hwang, S.W.1    Cho, K.J.2    Kang, J.H.3
  • 27
    • 0033972847 scopus 로고    scopus 로고
    • Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome
    • Konig A., Happle R., Bornholdt E., et al. Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome. Am J Med Genet 2000, 90:339-346.
    • (2000) Am J Med Genet , vol.90 , pp. 339-346
    • Konig, A.1    Happle, R.2    Bornholdt, E.3
  • 28
    • 0036553657 scopus 로고    scopus 로고
    • A novel missense mutation of NSDHL in an unusual case of CHILD syndrome showing bilateral, almost symmetric involvement
    • Fink-Puches
    • Konig A., Happle R., Fink-Puches, et al. A novel missense mutation of NSDHL in an unusual case of CHILD syndrome showing bilateral, almost symmetric involvement. J Am Acad Dermatol 2002, 46:594-596.
    • (2002) J Am Acad Dermatol , vol.46 , pp. 594-596
    • Konig, A.1    Happle, R.2
  • 29
    • 33646693868 scopus 로고    scopus 로고
    • X-chromosome inactivation: role in skin disease expression
    • Happle R. X-chromosome inactivation: role in skin disease expression. Acta Paediatr 2006, 95:16-23.
    • (2006) Acta Paediatr , vol.95 , pp. 16-23
    • Happle, R.1
  • 30
    • 34347366264 scopus 로고    scopus 로고
    • Wnt signaling in focal dermal hypoplasia
    • Paller A.S. Wnt signaling in focal dermal hypoplasia. Nat Genet 2007, 39:820-821.
    • (2007) Nat Genet , vol.39 , pp. 820-821
    • Paller, A.S.1
  • 31
    • 34248597235 scopus 로고    scopus 로고
    • Keratin 1 gene mutation detected in epidermal nevus with epidermolytic hyperkeratosis
    • Tsubota A., Akiyama M., Sakai K., et al. Keratin 1 gene mutation detected in epidermal nevus with epidermolytic hyperkeratosis. J Invest Dermatol 2007, 127:1371-1374.
    • (2007) J Invest Dermatol , vol.127 , pp. 1371-1374
    • Tsubota, A.1    Akiyama, M.2    Sakai, K.3
  • 32
    • 0034526292 scopus 로고    scopus 로고
    • Mosaicism for ATP2A2 mutations causes segmental Darier's disease
    • Sakuntabhai A., Dhitavat J., Burge S., et al. Mosaicism for ATP2A2 mutations causes segmental Darier's disease. J Invest Dermatol 2000, 115:1144-1147.
    • (2000) J Invest Dermatol , vol.115 , pp. 1144-1147
    • Sakuntabhai, A.1    Dhitavat, J.2    Burge, S.3
  • 33
    • 0034080551 scopus 로고    scopus 로고
    • Segmental neurofibromatosis is caused by somatic mutations of neurofibromatosis type 1 (NF1) gene
    • Tinscher S., Naumann I., Stegmann E., et al. Segmental neurofibromatosis is caused by somatic mutations of neurofibromatosis type 1 (NF1) gene. Eur J Hum Genet 2000, 8:455-459.
    • (2000) Eur J Hum Genet , vol.8 , pp. 455-459
    • Tinscher, S.1    Naumann, I.2    Stegmann, E.3
  • 34
    • 0032578269 scopus 로고    scopus 로고
    • Epidermal mosaicism producing localized acne: somatic mutation in FGFR2
    • Munro C.S., Wilkie A.O. Epidermal mosaicism producing localized acne: somatic mutation in FGFR2. Lancet 1998, 352:704-705.
    • (1998) Lancet , vol.352 , pp. 704-705
    • Munro, C.S.1    Wilkie, A.O.2
  • 35
    • 43749121346 scopus 로고    scopus 로고
    • Unilateral segmental acneiform naevus: a model disorder towards understanding fibroblast growth factor receptor 2 function in acne?
    • Melnik B.C., Vakilzadeh F., Aslanidis C., et al. Unilateral segmental acneiform naevus: a model disorder towards understanding fibroblast growth factor receptor 2 function in acne?. Br J Dermatol 2008, 158:1397-1399.
    • (2008) Br J Dermatol , vol.158 , pp. 1397-1399
    • Melnik, B.C.1    Vakilzadeh, F.2    Aslanidis, C.3
  • 36
    • 33746754183 scopus 로고    scopus 로고
    • Mosaicism of activating of activating FGFR3 mutations in human skin causes epidermal nevi
    • Hafner C., van Oers J.M.M., Vogt T., et al. Mosaicism of activating of activating FGFR3 mutations in human skin causes epidermal nevi. J Clin Invest 2006, 116(33):744-748.
    • (2006) J Clin Invest , vol.116 , Issue.33 , pp. 744-748
    • Hafner, C.1    van Oers, J.M.M.2    Vogt, T.3
  • 37
    • 51449101662 scopus 로고    scopus 로고
    • An epidermal nevus syndrome with cerebral involvement caused by a mosaic FGFR3 mutation
    • Garcia-Vargas A., Hafner C., Perez Rodrigez A.G., et al. An epidermal nevus syndrome with cerebral involvement caused by a mosaic FGFR3 mutation. Am J Med Genet 2008, 146A:2275-2279.
    • (2008) Am J Med Genet , vol.146 A , pp. 2275-2279
    • Garcia-Vargas, A.1    Hafner, C.2    Perez Rodrigez, A.G.3
  • 38
    • 2142737884 scopus 로고    scopus 로고
    • A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus
    • Terrinoni A., Puddu P., Didona B., et al. A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus. J Invest Dermatol 2000, 114:1136-1140.
    • (2000) J Invest Dermatol , vol.114 , pp. 1136-1140
    • Terrinoni, A.1    Puddu, P.2    Didona, B.3
  • 39
    • 58149152854 scopus 로고    scopus 로고
    • Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations
    • Limaye N., Wouters V., Uebelhoer M., et al. Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations. Nat Genet 2009, 41:118-124.
    • (2009) Nat Genet , vol.41 , pp. 118-124
    • Limaye, N.1    Wouters, V.2    Uebelhoer, M.3
  • 40
    • 85047694384 scopus 로고    scopus 로고
    • Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept
    • Poblete-Gutierrez P., Wiederholt T., Konig A., et al. Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept. J Clin Invest 2004, 114:1407-1409.
    • (2004) J Clin Invest , vol.114 , pp. 1407-1409
    • Poblete-Gutierrez, P.1    Wiederholt, T.2    Konig, A.3
  • 41
    • 34547796898 scopus 로고    scopus 로고
    • Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1
    • Maertens O., De Schepper S., Vandesompele J., et al. Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1. Am J Hum Genet 2007, 81:243-251.
    • (2007) Am J Hum Genet , vol.81 , pp. 243-251
    • Maertens, O.1    De Schepper, S.2    Vandesompele, J.3
  • 42
    • 34548328245 scopus 로고    scopus 로고
    • Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype
    • Brems H., Chmara M., Sahbatou M., et al. Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype. Nat Genet 2007, 39:1120-1126.
    • (2007) Nat Genet , vol.39 , pp. 1120-1126
    • Brems, H.1    Chmara, M.2    Sahbatou, M.3
  • 43
    • 34250708389 scopus 로고    scopus 로고
    • Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity
    • Caux F., Plauchu H., Chibon F., et al. Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity. Eur J Hum Genet 2007, 15:767-773.
    • (2007) Eur J Hum Genet , vol.15 , pp. 767-773
    • Caux, F.1    Plauchu, H.2    Chibon, F.3
  • 44
    • 0036201378 scopus 로고    scopus 로고
    • Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas")
    • Brouillard P., Boon L.M., Mulliken J.B., et al. Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas"). Am J Hum Genet 2002, 70:866-874.
    • (2002) Am J Hum Genet , vol.70 , pp. 866-874
    • Brouillard, P.1    Boon, L.M.2    Mulliken, J.B.3
  • 45
    • 28844473140 scopus 로고    scopus 로고
    • Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's syndrome)
    • Ritzmann S., Hanneken S., Neumann N.J., et al. Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's syndrome). Dermatology 2006, 212:84-87.
    • (2006) Dermatology , vol.212 , pp. 84-87
    • Ritzmann, S.1    Hanneken, S.2    Neumann, N.J.3
  • 46
    • 34548537698 scopus 로고    scopus 로고
    • Type 2 segmental trichoepitheliomatosis: a genetic concept that may explain congenital multiple trichoepitheliomas in the lines of Blaschko
    • Happle R. Type 2 segmental trichoepitheliomatosis: a genetic concept that may explain congenital multiple trichoepitheliomas in the lines of Blaschko. Pediatr Dermatol 2007, 24:448-449.
    • (2007) Pediatr Dermatol , vol.24 , pp. 448-449
    • Happle, R.1
  • 47
    • 0025805216 scopus 로고
    • Somatic recombination may explain linear porokeratosis associated with disseminated superficial actinic porokeratosis
    • Happle R. Somatic recombination may explain linear porokeratosis associated with disseminated superficial actinic porokeratosis. Am J Med Genet 1991, 39:237.
    • (1991) Am J Med Genet , vol.39 , pp. 237
    • Happle, R.1
  • 48
    • 69749084897 scopus 로고    scopus 로고
    • What is paradominant inheritance?
    • Happle R. What is paradominant inheritance?. J Med Genet 2009, 46:648.
    • (2009) J Med Genet , vol.46 , pp. 648
    • Happle, R.1
  • 50
    • 0031466163 scopus 로고    scopus 로고
    • Trimethoprim-induced linear fixed drug eruption
    • Ozkaya-Bayazit E., Baykal C. Trimethoprim-induced linear fixed drug eruption. Br J Dermatol 1997, 137:1028.1-1029.1.
    • (1997) Br J Dermatol , vol.137
    • Ozkaya-Bayazit, E.1    Baykal, C.2
  • 52
    • 0035683775 scopus 로고    scopus 로고
    • Generalized lichenoid drug eruption following Blaschko lines
    • Krasowska D., Schwartz R.A., Lecewicz-Torun B. Generalized lichenoid drug eruption following Blaschko lines. Int J Dermatol 2001, 40:774-776.
    • (2001) Int J Dermatol , vol.40 , pp. 774-776
    • Krasowska, D.1    Schwartz, R.A.2    Lecewicz-Torun, B.3
  • 53
    • 0041856219 scopus 로고    scopus 로고
    • Linear atrophoderma of Moulin: postulation of mosaicism for a predisposing gene
    • Danarti R., Bittar M., Happle R., et al. Linear atrophoderma of Moulin: postulation of mosaicism for a predisposing gene. J Acad Dermatol 2003, 49:492-498.
    • (2003) J Acad Dermatol , vol.49 , pp. 492-498
    • Danarti, R.1    Bittar, M.2    Happle, R.3
  • 54
    • 26644469842 scopus 로고    scopus 로고
    • Atopic dermatitis with increased severity along a line of Blaschko
    • Hladik F., Jurecka W., Hayek B., et al. Atopic dermatitis with increased severity along a line of Blaschko. J Am Acad Dermatol 2005, 53:S221-224.
    • (2005) J Am Acad Dermatol , vol.53
    • Hladik, F.1    Jurecka, W.2    Hayek, B.3
  • 55
    • 67049088530 scopus 로고    scopus 로고
    • Linear cutaneous lupus erythematosus: a subset of childhood cutaneous lupus erythematosus
    • Gaitanis G., Nomikos K., Chaniotakis I., et al. Linear cutaneous lupus erythematosus: a subset of childhood cutaneous lupus erythematosus. Lupus 2009, 18:759-761.
    • (2009) Lupus , vol.18 , pp. 759-761
    • Gaitanis, G.1    Nomikos, K.2    Chaniotakis, I.3
  • 56
    • 45749090861 scopus 로고    scopus 로고
    • Linear morphoea follows Blaschko's lines
    • Weibel L., Harper J.I. Linear morphoea follows Blaschko's lines. Br J Dermatol 2008, 159:175-181.
    • (2008) Br J Dermatol , vol.159 , pp. 175-181
    • Weibel, L.1    Harper, J.I.2
  • 57
    • 2942557219 scopus 로고    scopus 로고
    • Lichen striatus: clinical and laboratory features of 115 children
    • Patrizi A., Neri I., Fiorentini C., et al. Lichen striatus: clinical and laboratory features of 115 children. Pediatr Dermatol 2004, 21:197-204.
    • (2004) Pediatr Dermatol , vol.21 , pp. 197-204
    • Patrizi, A.1    Neri, I.2    Fiorentini, C.3
  • 59
    • 10244247772 scopus 로고    scopus 로고
    • Acquired Blaschko dermatitis: acquired relapsing self-healing Blaschko dermatitis
    • Lee H.J., Kang W.H., Hann S.K. Acquired Blaschko dermatitis: acquired relapsing self-healing Blaschko dermatitis. J Dermatol 1996, 23:639-642.
    • (1996) J Dermatol , vol.23 , pp. 639-642
    • Lee, H.J.1    Kang, W.H.2    Hann, S.K.3
  • 60
    • 36448940857 scopus 로고    scopus 로고
    • Fangman W, et al. "Pediatric blaschkitis": expanding the spectrum of childhood acquired Blaschko-linear dermatoses
    • Keegan B.R., Kamino H. Fangman W, et al. "Pediatric blaschkitis": expanding the spectrum of childhood acquired Blaschko-linear dermatoses. Pediatr Dermatol 2007, 24:621-627.
    • (2007) Pediatr Dermatol , vol.24 , pp. 621-627
    • Keegan, B.R.1    Kamino, H.2
  • 61
    • 32944465293 scopus 로고    scopus 로고
    • Linear psoriasis and ILVEN: is lumping or splitting appropriate
    • Happle R. Linear psoriasis and ILVEN: is lumping or splitting appropriate. Dermatology 2006, 212:101-102.
    • (2006) Dermatology , vol.212 , pp. 101-102
    • Happle, R.1
  • 62
    • 0035657308 scopus 로고    scopus 로고
    • Inflammatory linear verrucous epidermal naevi: a review of 23 cases
    • Lee S.H., Rogers M. Inflammatory linear verrucous epidermal naevi: a review of 23 cases. Australas J Dermatol 2001, 42:252-256.
    • (2001) Australas J Dermatol , vol.42 , pp. 252-256
    • Lee, S.H.1    Rogers, M.2
  • 63
    • 71549121638 scopus 로고    scopus 로고
    • Widespread porokeratotic adnexal ostial nevus: clinical features and proposal of a new name unifying porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus
    • Goddard D.S., Rogers M., Frieden I.J., et al. Widespread porokeratotic adnexal ostial nevus: clinical features and proposal of a new name unifying porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus. J Am Acad Dermatol 2009, 61:1060.e1-1060.e14.
    • (2009) J Am Acad Dermatol , vol.61
    • Goddard, D.S.1    Rogers, M.2    Frieden, I.J.3
  • 64
    • 4544268599 scopus 로고    scopus 로고
    • Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes
    • Taibjee S.M., Moss C. Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes. Br J Dermatol 2004, 151:269-282.
    • (2004) Br J Dermatol , vol.151 , pp. 269-282
    • Taibjee, S.M.1    Moss, C.2
  • 65
    • 0029854056 scopus 로고    scopus 로고
    • Analysis of 54 cases of hypopigmentation and hyperpigmentation along the lines of Blaschko
    • Nehal K.S., Pebenito R., Orlow S.J. Analysis of 54 cases of hypopigmentation and hyperpigmentation along the lines of Blaschko. Arch Dermatol 1996, 132:1167-1170.
    • (1996) Arch Dermatol , vol.132 , pp. 1167-1170
    • Nehal, K.S.1    Pebenito, R.2    Orlow, S.J.3
  • 66
    • 0344223304 scopus 로고    scopus 로고
    • Hypomelanosis of Ito: no entity, but a cutaneous sign of mosaicism
    • Küster W., König A. Hypomelanosis of Ito: no entity, but a cutaneous sign of mosaicism. Am J Med Genet 1999, 85:346-350.
    • (1999) Am J Med Genet , vol.85 , pp. 346-350
    • Küster, W.1    König, A.2
  • 67
    • 0026528367 scopus 로고
    • Hypomelanosis of Ito: diagnostic criteria and report of 41 cases
    • Ruiz-Maldonado R., Toussaint S., Tamayo L., et al. Hypomelanosis of Ito: diagnostic criteria and report of 41 cases. Pediatr Dermatol 1992, 9:1-10.
    • (1992) Pediatr Dermatol , vol.9 , pp. 1-10
    • Ruiz-Maldonado, R.1    Toussaint, S.2    Tamayo, L.3
  • 68
    • 0030391746 scopus 로고    scopus 로고
    • Prevalence of hypopigmented macules in a healthy population
    • Vanderhooft S.L., Francis J.S., Pagon R.A., et al. Prevalence of hypopigmented macules in a healthy population. J Pediatr 1996, 1229:355-361.
    • (1996) J Pediatr , vol.1229 , pp. 355-361
    • Vanderhooft, S.L.1    Francis, J.S.2    Pagon, R.A.3
  • 69
    • 0033006378 scopus 로고    scopus 로고
    • Nevus depigmentosus: clinical features and histopathological characteristics in 67 patients
    • Lee H.S., Chun Y.S., Hann S.K. Nevus depigmentosus: clinical features and histopathological characteristics in 67 patients. J Am Acad Dermatol 1999, 40:21-26.
    • (1999) J Am Acad Dermatol , vol.40 , pp. 21-26
    • Lee, H.S.1    Chun, Y.S.2    Hann, S.K.3
  • 70
    • 33746876726 scopus 로고    scopus 로고
    • Clinical and histopathologic characteristics of nevus depigmentosus
    • Kim S.K., Kang H.Y., Lee E.S., et al. Clinical and histopathologic characteristics of nevus depigmentosus. J Am Acad Dermatol 2006, 55:423-428.
    • (2006) J Am Acad Dermatol , vol.55 , pp. 423-428
    • Kim, S.K.1    Kang, H.Y.2    Lee, E.S.3
  • 71
    • 45149108291 scopus 로고    scopus 로고
    • Clinical, histopathological and ultrastructural characteristics of naevus depigmentosus
    • Xu A.E., Huang B., Li Y.W., et al. Clinical, histopathological and ultrastructural characteristics of naevus depigmentosus. Clin Exp Dermatol 2008, 33:400-405.
    • (2008) Clin Exp Dermatol , vol.33 , pp. 400-405
    • Xu, A.E.1    Huang, B.2    Li, Y.W.3
  • 72
    • 0036117871 scopus 로고    scopus 로고
    • Prevalence of hypopigmented maculae and café-au-lait spots in idiopathic epileptic and healthy children
    • Karabiber H., Sasmaz S., Turanli G., et al. Prevalence of hypopigmented maculae and café-au-lait spots in idiopathic epileptic and healthy children. J Child Neurol 2002, 17:57-59.
    • (2002) J Child Neurol , vol.17 , pp. 57-59
    • Karabiber, H.1    Sasmaz, S.2    Turanli, G.3
  • 73
    • 23344448096 scopus 로고    scopus 로고
    • Mosaicism in cutaneous pigmentation
    • Lombillo V.A., Sybert V.P. Mosaicism in cutaneous pigmentation. Curr Opin Ped 2005, 17:494-500.
    • (2005) Curr Opin Ped , vol.17 , pp. 494-500
    • Lombillo, V.A.1    Sybert, V.P.2
  • 74
    • 34249813140 scopus 로고    scopus 로고
    • Linear and whorled hypermelanosis
    • Di Lernia V. Linear and whorled hypermelanosis. Pediatr Dermatol 2007, 24:205-210.
    • (2007) Pediatr Dermatol , vol.24 , pp. 205-210
    • Di Lernia, V.1
  • 75
    • 16344394789 scopus 로고    scopus 로고
    • X-linked reticulate pigmentary disorder with systemic manifestations: report of a third family and literature review
    • Anderson R.C., Zinn A.R., Kim J., et al. X-linked reticulate pigmentary disorder with systemic manifestations: report of a third family and literature review. Pediatr Dermatol 2005, 22:122-126.
    • (2005) Pediatr Dermatol , vol.22 , pp. 122-126
    • Anderson, R.C.1    Zinn, A.R.2    Kim, J.3
  • 76
    • 0033952715 scopus 로고    scopus 로고
    • Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia
    • Cambiaghi S., Restano L., Pääkkönen K., et al. Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia. Arch Dermatol 2000, 136:217-224.
    • (2000) Arch Dermatol , vol.136 , pp. 217-224
    • Cambiaghi, S.1    Restano, L.2    Pääkkönen, K.3
  • 77
    • 0034891223 scopus 로고    scopus 로고
    • Female patient showing hypohidrotic ectodermal dysplasia and immunodeficiency
    • Kosaki K., Shimasaki N., Fukushima H., et al. Female patient showing hypohidrotic ectodermal dysplasia and immunodeficiency. Am J Hum Genet 2001, 69:664-665.
    • (2001) Am J Hum Genet , vol.69 , pp. 664-665
    • Kosaki, K.1    Shimasaki, N.2    Fukushima, H.3
  • 78
    • 0030958069 scopus 로고    scopus 로고
    • Linear hypopigmentation and hyperpigmentation including mosaicism
    • Loomis C.A. Linear hypopigmentation and hyperpigmentation including mosaicism. Semin Cutan Med Surg 1997, 16:44-53.
    • (1997) Semin Cutan Med Surg , vol.16 , pp. 44-53
    • Loomis, C.A.1
  • 79
    • 33847004020 scopus 로고    scopus 로고
    • Heterochromia of the scalp hair following Blaschko lines
    • Iorizzo M., Piraccini B.M., Tosti A. Heterochromia of the scalp hair following Blaschko lines. Pediatr Dermatol 2007, 24:69-70.
    • (2007) Pediatr Dermatol , vol.24 , pp. 69-70
    • Iorizzo, M.1    Piraccini, B.M.2    Tosti, A.3
  • 80
    • 0032777704 scopus 로고    scopus 로고
    • Loss of heterozygosity in human skin
    • Happle R. Loss of heterozygosity in human skin. J Am Acad Dermatol 1999, 41:143-161.
    • (1999) J Am Acad Dermatol , vol.41 , pp. 143-161
    • Happle, R.1
  • 81
    • 0034821788 scopus 로고    scopus 로고
    • Recombinogenic activity of four compounds in the standard and high bioactivation crosses of Drosophila melanogaster in the wing spot test
    • Spano M.A., Frei H., Wurgler F.E., et al. Recombinogenic activity of four compounds in the standard and high bioactivation crosses of Drosophila melanogaster in the wing spot test. Mutagenesis 2001, 16:285-294.
    • (2001) Mutagenesis , vol.16 , pp. 285-294
    • Spano, M.A.1    Frei, H.2    Wurgler, F.E.3
  • 82
    • 14944378165 scopus 로고    scopus 로고
    • Phacomatosis pigmentovascularis revisited and reclassified
    • Happle R. Phacomatosis pigmentovascularis revisited and reclassified. Arch Dermatol 2005, 141:385-388.
    • (2005) Arch Dermatol , vol.141 , pp. 385-388
    • Happle, R.1


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