메뉴 건너뛰기




Volumn 10, Issue 6, 2009, Pages 351-364

Ichthyosis: Clinical manifestations and practical treatment options

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL; ANTIINFECTIVE AGENT; DEXPANTHENOL; ETRETIN; GLYCEROL; HUMECTANT; KERATOLYTIC AGENT; LACTIC ACID; LIAROZOLE; PROPYLENE GLYCOL; RETINOIC ACID; RETINOID; SALICYLIC ACID; SODIUM CHLORIDE; TAZAROTENE; UREA; XIPAMIDE;

EID: 70350340708     PISSN: 11750561     EISSN: 11791888     Source Type: Journal    
DOI: 10.2165/11311070-000000000-00000     Document Type: Review
Times cited : (109)

References (79)
  • 2
    • 33748333074 scopus 로고    scopus 로고
    • Ichthyoses: Differential diagnosis and molecular genetics
    • Oji V, Traupe H. Ichthyoses: differential diagnosis and molecular genetics. Eur J Dermatol 2006; 16: 349-359
    • (2006) Eur J Dermatol , vol.16 , pp. 349-359
    • Oji, V.1    Traupe, H.2
  • 3
    • 70350305170 scopus 로고    scopus 로고
    • Revised nomenclature and classification of inherited ichthyoses
    • Jan 23-24; Sorè ze [online]. Available from URL [Accessed 2009 Sep 21]
    • Oji, V, Tadini, G, Akiyama, M, et al. Revised nomenclature and classification of inherited ichthyoses. Ichthyosis Consensus Conference; 2009 Jan 23-24; Sorè ze [online]. Available from URL: http://www.netzwerk- ichthyose.de/ index.php?id=28&L=1 [Accessed 2009 Sep 21]
    • (2009) Ichthyosis Consensus Conference
    • Oji, V.1    Tadini, G.2    Akiyama, M.3
  • 4
    • 70350308239 scopus 로고    scopus 로고
    • Update of themoderation process of the ichthyosis classification
    • Jan 23-24; Sorè ze [online]. Available from URL [Accessed 2009 Sep 21]
    • OjiV.Update of themoderation process of the ichthyosis classification. Ichthyosis Consensus Conference; 2009 Jan 23-24; Sorè ze [online]. Available from URL: http://www.netzwerk-ichthyose.de/index.php?id=28&L=1 [Accessed 2009 Sep 21].
    • (2009) Ichthyosis Consensus Conference
    • Oji, V.1
  • 5
    • 70350287179 scopus 로고    scopus 로고
    • Classification of congenital ichthyosis
    • Aug 31-Sep 2; Münster
    • Classification of congenital ichthyosis. First World Conference on Ichthyosis; 2007 Aug 31-Sep 2; Münster
    • (2007) First World Conference on Ichthyosis
  • 6
    • 44949151890 scopus 로고    scopus 로고
    • Thematic review series: Skin lipids. Pathogenesis of permeability barrier abnormalities in the ichthyoses: Inherited disorders of lipid metabolism
    • Elias PM, Williams ML, Holleran WM, et al. Thematic review series: skin lipids. Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism. J Lipid Res 2008; 49: 697-714
    • (2008) J Lipid Res , vol.49 , pp. 697-714
    • Elias, P.M.1    Williams, M.L.2    Holleran, W.M.3
  • 7
    • 36048949627 scopus 로고    scopus 로고
    • Ichthyosis update: Towards a functiondriven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders
    • SchmuthM, Gruber R, Elias PM, et al. Ichthyosis update: towards a functiondriven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders. Adv Dermatol 2007; 23: 231-256
    • (2007) Adv Dermatol , vol.23 , pp. 231-256
    • Schmuthm Gruber, R.1    Elias, P.M.2
  • 8
    • 3042812660 scopus 로고    scopus 로고
    • Ichthyosiform dermatoses: So many discoveries, so little progress
    • DiGiovanna JJ. Ichthyosiform dermatoses: so many discoveries, so little progress. J Am Acad Dermatol 2004; 51: S31-4
    • (2004) J Am Acad Dermatol , vol.51
    • Digiovanna, J.J.1
  • 9
    • 0013791601 scopus 로고
    • Genetic classification of ichthyosis
    • Wells RS, Kerr CB. Genetic classification of ichthyosis. Arch Dermatol 1965; 92: 1-6
    • (1965) Arch Dermatol , vol.92 , pp. 1-6
    • Wells, R.S.1    Kerr, C.B.2
  • 10
    • 0014194586 scopus 로고
    • X-linked ichthyosis and ichthyosis vulgaris: Clinical and genetic distinctions in a second series of families
    • Wells RS, Jennings MC. X-linked ichthyosis and ichthyosis vulgaris: clinical and genetic distinctions in a second series of families. JAMA 1967; 202: 485-488
    • (1967) JAMA , vol.202 , pp. 485-488
    • Wells, R.S.1    Jennings, M.C.2
  • 11
    • 33644622891 scopus 로고    scopus 로고
    • Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris
    • Smith FJ, Irvine AD, Terron-Kwiatkowski A, et al. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. NatGenet 2006; 38: 337-342
    • (2006) NatGenet , vol.38 , pp. 337-342
    • Smith, F.J.1    Irvine, A.D.2    Terron-Kwiatkowski, A.3
  • 12
    • 36248957531 scopus 로고    scopus 로고
    • Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis
    • Liao H, Waters AJ, Goudie DR, et al. Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis. J Invest Dermatol 2007; 127: 2795-2798
    • (2007) J Invest Dermatol , vol.127 , pp. 2795-2798
    • Liao, H.1    Waters, A.J.2    Goudie, D.R.3
  • 13
    • 84919585371 scopus 로고
    • X-linked ichthyosis due to steroidsulphatase deficiency
    • Webster D, France JT, Shapiro LJ, et al. X-linked ichthyosis due to steroidsulphatase deficiency. Lancet 1978; I: 70-72
    • (1978) Lancet , vol.1 , pp. 70-72
    • Webster, D.1    France, J.T.2    Shapiro, L.J.3
  • 14
    • 1842283931 scopus 로고
    • Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis
    • USA
    • Ballabio A, Parenti G, Carrozzo R, et al. Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis. Proc Natl Acad SciUSA1987; 84: 4519-4523
    • (1987) Proc Natl Acad Sci , vol.84 , pp. 4519-4523
    • Ballabio, A.1    Parenti, G.2    Carrozzo, R.3
  • 16
    • 34547776343 scopus 로고    scopus 로고
    • Compound heterozygous ABCA12 mutations including a novel nonsense mutation underlie harlequin ichthyosis
    • Akiyama M, Sakai K, Sato T, et al. Compound heterozygous ABCA12 mutations including a novel nonsense mutation underlie harlequin ichthyosis. Dermatology 2007; 215: 155-159
    • (2007) Dermatology , vol.215 , pp. 155-159
    • Akiyama, M.1    Sakai, K.2    Sato, T.3
  • 17
    • 20244379129 scopus 로고    scopus 로고
    • Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis
    • Kelsell DP, Norgett EE, Unsworth H, et al. Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis. Am J Hum Genet 2005; 76: 794-803
    • (2005) Am J Hum Genet , vol.76 , pp. 794-803
    • Kelsell, D.P.1    Norgett, E.E.2    Unsworth, H.3
  • 18
    • 10744220980 scopus 로고    scopus 로고
    • Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2
    • Lefevre C, Audebert S, Jobard F, et al.Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2. Hum Mol Genet 2003; 12: 2369-2378
    • (2003) Hum Mol Genet , vol.12 , pp. 2369-2378
    • Lefevre, C.1    Audebert, S.2    Jobard, F.3
  • 19
    • 0038115548 scopus 로고    scopus 로고
    • The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis
    • Akiyama M, Sawamura D, Shimizu H. The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis. Clin Exp Dermatol 2003; 28: 235-240
    • (2003) Clin Exp Dermatol , vol.28 , pp. 235-240
    • Akiyama, M.1    Sawamura, D.2    Shimizu, H.3
  • 20
    • 33750220685 scopus 로고    scopus 로고
    • Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: Evidence for a temperature-sensitive phenotype
    • Oji V, Hautier JM, Ahvazi B, et al. Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype. Hum Mol Genet 2006; 15: 3083-3097
    • (2006) Hum Mol Genet , vol.15 , pp. 3083-3097
    • Oji, V.1    Hautier, J.M.2    Ahvazi, B.3
  • 21
    • 0037313061 scopus 로고    scopus 로고
    • Self-healing collodion baby: A dynamic phenotype explained by a particular transglutaminase-1 mutation
    • Raghunath M, Hennies HC, Ahvazi B, et al. Self-healing collodion baby: a dynamic phenotype explained by a particular transglutaminase-1 mutation. J Invest Dermatol 2003; 120: 224-228
    • (2003) J Invest Dermatol , vol.120 , pp. 224-228
    • Raghunath, M.1    Hennies, H.C.2    Ahvazi, B.3
  • 22
    • 41149096095 scopus 로고    scopus 로고
    • Self-healing collodionmembrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene
    • HartingM, Brunetti-PierriN, Chan CS, et al. Self-healing collodionmembrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene. Arch Dermatol 2008; 144: 351-356
    • (2008) Arch Dermatol , vol.144 , pp. 351-356
    • Brunetti-Pierrin, H.1    Chan, C.S.2
  • 23
    • 33144486941 scopus 로고    scopus 로고
    • Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3
    • Lefevre C, Bouadjar B, Ferrand V, et al. Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3. Hum Mol Genet 2006; 15: 767-776
    • (2006) Hum Mol Genet , vol.15 , pp. 767-776
    • Lefevre, C.1    Bouadjar, B.2    Ferrand, V.3
  • 24
    • 18244388249 scopus 로고    scopus 로고
    • Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1
    • Jobard F, Lefevre C, Karaduman A, et al. Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1. Hum Mol Genet 2002; 11: 107-113
    • (2002) Hum Mol Genet , vol.11 , pp. 107-113
    • Jobard, F.1    Lefevre, C.2    Karaduman, A.3
  • 25
    • 19544366925 scopus 로고    scopus 로고
    • Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis
    • Lefevre C, Bouadjar B, Karaduman A, et al. Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis. Hum Mol Genet 2004; 13: 2473-2482
    • (2004) Hum Mol Genet , vol.13 , pp. 2473-2482
    • Lefevre, C.1    Bouadjar, B.2    Karaduman, A.3
  • 26
    • 17444449599 scopus 로고
    • Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q
    • Compton JG, DiGiovanna JJ, Santucci SK, et al. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q. Nat Genet 1992; 1: 301-305
    • (1992) Nat Genet , vol.1 , pp. 301-305
    • Compton, J.G.1    Digiovanna, J.J.2    Santucci, S.K.3
  • 27
    • 0026781694 scopus 로고
    • Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis
    • Rothnagel JA, Dominey AM, Dempsey LD, et al. Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis. Science 1992; 257: 1128-1130
    • (1992) Science , vol.257 , pp. 1128-1130
    • Rothnagel, J.A.1    Dominey, A.M.2    Dempsey, L.D.3
  • 29
    • 84984777129 scopus 로고    scopus 로고
    • Refsum disease is caused by mutations in the phytanoyl-CoAhydroxylase gene
    • Jansen GA, Ofman R, Ferdinandusse S, et al. Refsum disease is caused by mutations in the phytanoyl-CoAhydroxylase gene. NatGenet 1997; 17: 190-193
    • (1997) NatGenet , vol.17 , pp. 190-193
    • Jansen, G.A.1    Ofman, R.2    Ferdinandusse, S.3
  • 30
    • 1542724509 scopus 로고    scopus 로고
    • Molecular basis of Refsum disease: Sequence variations in phytanoyl-CoA hydroxylase (PHYH) and the PTS2 receptor (PEX7)
    • Jansen GA, Waterham HR, Wanders RJ. Molecular basis of Refsum disease: sequence variations in phytanoyl-CoA hydroxylase (PHYH) and the PTS2 receptor (PEX7). Hum Mutat 2004; 23: 209-218
    • (2004) Hum Mutat , vol.23 , pp. 209-218
    • Jansen, G.A.1    Waterham, H.R.2    Wanders, R.J.3
  • 31
    • 0014028658 scopus 로고
    • Dietary effects on serum-phytanic-acid levels and on clinical manifestations in heredopathia atactica polyneuritiformis
    • Eldjarn L, TryK, Stokke O, et al. Dietary effects on serum-phytanic-acid levels and on clinical manifestations in heredopathia atactica polyneuritiformis. Lancet 1966; I: 691-693
    • (1966) Lancet , vol.1 , pp. 691-693
    • Eldjarn, L.1    Tryk Stokke, O.2
  • 32
    • 0035723116 scopus 로고    scopus 로고
    • The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: Implications for mutation detection and first case of prenatal diagnosis
    • Sprecher E, Chavanas S, DiGiovanna JJ, et al. The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosis. J Invest Dermatol 2001; 117: 179-187
    • (2001) J Invest Dermatol , vol.117 , pp. 179-187
    • Sprecher, E.1    Chavanas, S.2    Digiovanna, J.J.3
  • 33
    • 0034120666 scopus 로고    scopus 로고
    • Mutations in SPINK5 encoding a serine protease inhibitor causeNetherton syndrome
    • Chavanas S, Bodemer C, Rochat A, et al. Mutations in SPINK5, encoding a serine protease inhibitor, causeNetherton syndrome.Nat Genet 2000; 25: 141-142
    • (2000) Nat Genet , vol.25 , pp. 141-142
    • Chavanas, S.1    Bodemer, C.2    Rochat, A.3
  • 34
    • 0036125197 scopus 로고    scopus 로고
    • Elevated stratum corneum hydrolytic activity in Netherton syndrome suggests an inhibitory regulation of desquamation by SPINK5-derived peptides
    • Komatsu N, Takata M, Otsuki N, et al. Elevated stratum corneum hydrolytic activity in Netherton syndrome suggests an inhibitory regulation of desquamation by SPINK5-derived peptides. J Invest Dermatol 2002; 118: 436-443
    • (2002) J Invest Dermatol , vol.118 , pp. 436-443
    • Komatsu, N.1    Takata, M.2    Otsuki, N.3
  • 35
    • 0029664636 scopus 로고    scopus 로고
    • Sjogren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene
    • De Laurenzi V, Rogers GR, Hamrock DJ, et al. Sjogren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene. Nat Genet 1996; 12: 52-57
    • (1996) Nat Genet , vol.12 , pp. 52-57
    • De Laurenzi, V.1    Rogers, G.R.2    Hamrock, D.J.3
  • 36
    • 33847411888 scopus 로고    scopus 로고
    • Sjogren-Larsson syndrome
    • GordonN. Sjogren-Larsson syndrome. DevMed Child Neurol 2007; 49: 152-154
    • (2007) Dev Med Child Neurol , vol.49 , pp. 152-154
    • Gordon, N.1
  • 37
    • 0034764272 scopus 로고    scopus 로고
    • Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin- Dorfman syndrome
    • Lefevre C, Jobard F, Caux F, et al. Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin- Dorfman syndrome. Am J Hum Genet 2001; 69: 1002-1012
    • (2001) Am J Hum Genet , vol.69 , pp. 1002-1012
    • Lefevre, C.1    Jobard, F.2    Caux, F.3
  • 38
    • 0018895779 scopus 로고
    • Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidation
    • Angelini C, Philippart M, Borrone C, et al. Multisystem triglyceride storage disorder with impaired long-chain fatty acid oxidation. Ann Neurol 1980; 7: 5-10
    • (1980) Ann Neurol , vol.7 , pp. 5-10
    • Angelini, C.1    Philippart, M.2    Borrone, C.3
  • 39
    • 54049139573 scopus 로고    scopus 로고
    • Trichothiodystrophy: A systematic review of 112 published cases characterises a wide spectrum of clinical manifestations
    • Faghri S, Tamura D, Kraemer KH, et al. Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations. J Med Genet 2008; 45: 609-621
    • (2008) J Med Genet , vol.45 , pp. 609-621
    • Faghri, S.1    Tamura, D.2    Kraemer, K.H.3
  • 41
    • 0025020601 scopus 로고
    • Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: Variable morphology and structural protein expression and a defect in lamellar granules
    • Dale BA, Holbrook KA, Fleckman P, et al. Heterogeneity in harlequin ichthyosis, an inborn error of epidermal keratinization: variable morphology and structural protein expression and a defect in lamellar granules. J Invest Dermatol 1990; 94: 6-18
    • (1990) J Invest Dermatol , vol.94 , pp. 6-18
    • Dale, B.A.1    Holbrook, K.A.2    Fleckman, P.3
  • 42
    • 0021806009 scopus 로고
    • Neutral lipid storage disease with ichthyosis: Defective lamellar body contents and intracellular dispersion
    • Elias PM, Williams ML. Neutral lipid storage disease with ichthyosis: defective lamellar body contents and intracellular dispersion. Arch Dermatol 1985; 121: 1000-1008
    • (1985) Arch Dermatol , vol.121 , pp. 1000-1008
    • Elias, P.M.1    Williams, M.L.2
  • 43
    • 35348850047 scopus 로고    scopus 로고
    • Congenital ichthyosis: Mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis
    • Dahlqvist J, Klar J, Hausser I, et al. Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis. J Med Genet 2007; 44: 615-620
    • (2007) J Med Genet , vol.44 , pp. 615-620
    • Dahlqvist, J.1    Klar, J.2    Hausser, I.3
  • 44
    • 0344406729 scopus 로고    scopus 로고
    • In vivo studies of mutant keratin 1 in ichthyosis hystrix Curth-Macklin
    • Ishida-Yamamoto A, Richard G, Takahashi H, et al. In vivo studies of mutant keratin 1 in ichthyosis hystrix Curth-Macklin. J Invest Dermatol 2003; 120: 498-500
    • (2003) J Invest Dermatol , vol.120 , pp. 498-500
    • Ishida-Yamamoto, A.1    Richard, G.2    Takahashi, H.3    Al, E.4
  • 45
    • 11144294679 scopus 로고    scopus 로고
    • LEKTI demonstrable by immunohistochemistry of the skin: A potential diagnostic skin test for Netherton syndrome
    • Ong C, O'Toole EA, Ghali L, et al. LEKTI demonstrable by immunohistochemistry of the skin: a potential diagnostic skin test for Netherton syndrome. Br J Dermatol 2004; 151: 1253-1257
    • (2004) Br J Dermatol , vol.151 , pp. 1253-1257
    • Ong, C.1    O'Toole, E.A.2    Ghali, L.3
  • 46
    • 4143130046 scopus 로고    scopus 로고
    • SPINK5 and Netherton syndrome: Novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases
    • Raghunath M, Tontsidou L, Oji V, et al. SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases. J Invest Dermatol 2004; 123: 474-483
    • (2004) J Invest Dermatol , vol.123 , pp. 474-483
    • Raghunath, M.1    Tontsidou, L.2    Oji, V.3
  • 47
    • 0031788996 scopus 로고    scopus 로고
    • A novel in situ method for the detection of deficient transglutaminase activity in the skin
    • Raghunath M, Hennies HC, Velten F, et al. A novel in situ method for the detection of deficient transglutaminase activity in the skin. Arch Dermatol Res 1998; 290: 621-627
    • (1998) Arch Dermatol Res , vol.290 , pp. 621-627
    • Raghunath, M.1    Hennies, H.C.2    Velten, F.3
  • 48
    • 34247346974 scopus 로고    scopus 로고
    • Oral liarozole versus acitretin in the treatment of ichthyosis: A phase II/III multicentre, doubleblind, randomized, active-controlled study
    • Verfaille CJ, Vanhoutte FP, Blanchet-Bardon C, et al. Oral liarozole versus acitretin in the treatment of ichthyosis: a phase II/III multicentre, doubleblind, randomized, active-controlled study. Br J Dermatol 2007; 156: 965-973
    • (2007) Br J Dermatol , vol.156 , pp. 965-973
    • Verfaille, C.J.1    Vanhoutte, F.P.2    Blanchet-Bardon, C.3
  • 49
    • 0035054521 scopus 로고    scopus 로고
    • Assessment of the clinical effect of topical tacalcitol on ichthyoses with retentive hyperkeratosis
    • Okano M. Assessment of the clinical effect of topical tacalcitol on ichthyoses with retentive hyperkeratosis. Dermatology 2001; 202: 116-118
    • (2001) Dermatology , vol.202 , pp. 116-118
    • Okano, M.1
  • 50
    • 0031021596 scopus 로고    scopus 로고
    • Oral treatment of ichthyosis by the cytochrome P-450 inhibitor liarozole
    • Lucker GP, Heremans AM, Boegheim PJ, et al. Oral treatment of ichthyosis by the cytochrome P-450 inhibitor liarozole. Br J Dermatol 1997; 136: 71-75
    • (1997) Br J Dermatol , vol.136 , pp. 71-75
    • Lucker, G.P.1    Heremans, A.M.2    Boegheim, P.J.3
  • 51
    • 17444387774 scopus 로고    scopus 로고
    • Topical liarozole in ichthyosis: A double-blind, left-right comparative study followed by a long-term open maintenance study
    • Lucker GP, Verfaille CJ, Heremans AM, et al. Topical liarozole in ichthyosis: a double-blind, left-right comparative study followed by a long-term open maintenance study. Br J Dermatol 2005; 152: 566-569
    • (2005) Br J Dermatol , vol.152 , pp. 566-569
    • Lucker, G.P.1    Verfaille, C.J.2    Heremans, A.M.3
  • 52
    • 2642649487 scopus 로고    scopus 로고
    • Efficacy of urea therapy in children with ichthyosis: A multicenter randomized, placebo-controlled, double-blind, semilateral study
    • Kuster W, Bohnsack K, Rippke F, et al. Efficacy of urea therapy in children with ichthyosis: a multicenter randomized, placebo-controlled, double-blind, semilateral study. Dermatology 1998; 196: 217-222
    • (1998) Dermatology , vol.196 , pp. 217-222
    • Kuster, W.1    Bohnsack, K.2    Rippke, F.3
  • 53
    • 0029075736 scopus 로고
    • Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinization: Results of a randomized, double-blind, vehicle-controlled, right/left comparative study
    • Kragballe K, Steijlen PM, Ibsen HH, et al. Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinization: results of a randomized, double-blind, vehicle-controlled, right/left comparative study. Arch Dermatol 1995; 131: 556-560
    • (1995) Arch Dermatol , vol.131 , pp. 556-560
    • Kragballe, K.1    Steijlen, P.M.2    Ibsen, H.H.3
  • 54
    • 0032086073 scopus 로고    scopus 로고
    • An evaluation of the effect of an alpha hydroxy acid-blend skin cream in the cosmetic improvement of symptoms of moderate to severe xerosis, epidermolytic hyperkeratosis, and ichthyosis
    • Kempers S, Katz HI,Wildnauer R, et al. An evaluation of the effect of an alpha hydroxy acid-blend skin cream in the cosmetic improvement of symptoms of moderate to severe xerosis, epidermolytic hyperkeratosis, and ichthyosis. Cutis 1998; 61: 347-350
    • (1998) Cutis , vol.61 , pp. 347-350
    • Kempers, S.1    Katz Hiwildnauer, R.2
  • 55
    • 0033400536 scopus 로고    scopus 로고
    • Improved topical treatment of lamellar ichthyosis: A double-blind study of four different cream formulations
    • Ganemo A, Virtanen M, Vahlquist A. Improved topical treatment of lamellar ichthyosis: a double-blind study of four different cream formulations. Br J Dermatol 1999; 141: 1027-1032
    • (1999) Br J Dermatol , vol.141 , pp. 1027-1032
    • Ganemo, A.1    Virtanen, M.2    Vahlquist, A.3
  • 57
    • 33747233749 scopus 로고    scopus 로고
    • Ichthyoses: Suggestions for an improved therapy
    • Kuster W. Ichthyoses: suggestions for an improved therapy. Deutsches Arzteblatt 2006; 103: 1484-1489
    • (2006) Deutsches Arzteblatt , vol.103 , pp. 1484-1489
    • Kuster, W.1
  • 58
    • 1542283650 scopus 로고    scopus 로고
    • Disorders of keratinization: Diagnosis and management
    • Shwayder T. Disorders of keratinization: diagnosis and management. Am J Clin Dermatol 2004; 5: 17-29
    • (2004) Am J Clin Dermatol , vol.5 , pp. 17-29
    • Shwayder, T.1
  • 59
    • 70350259265 scopus 로고    scopus 로고
    • Treatment of ichthyosis: There is always something you can do! in memoriam: Wolfgang Küster
    • Traupe H, Burgdorf WHC. Treatment of ichthyosis: there is always something you can do! In memoriam: Wolfgang Küster. Am Acad Dermatol 2007; 57: 542-547
    • (2007) Am Acad Dermatol , vol.57 , pp. 542-547
    • Traupe, H.1    Burgdorf, W.H.C.2
  • 60
    • 38949159705 scopus 로고    scopus 로고
    • Congenital ichthyosis: An overview of current and emerging therapies
    • Vahlquist A, Ganemo A, Virtanen M. Congenital ichthyosis: an overview of current and emerging therapies. Acta Derm Venereol 2008; 88: 4-14
    • (2008) Acta Derm Venereol , vol.88 , pp. 4-14
    • Vahlquist, A.1    Ganemo, A.2    Virtanen, M.3
  • 61
    • 44949151890 scopus 로고    scopus 로고
    • Thematic review series: Skin lipids. Pathogenesis of permeability barrier abnormalities in the ichthyoses: Inherited disorders of lipid metabolism
    • Elias PM, Williams ML, Holleran WM, et al. Thematic review series: skin lipids. Pathogenesis of permeability barrier abnormalities in the ichthyoses: inherited disorders of lipid metabolism. J Lipid Res 2008; 49: 697-714
    • (2008) J Lipid Res , vol.49 , pp. 697-714
    • Elias, P.M.1    Williams, M.L.2    Holleran, W.M.3
  • 62
    • 0032716344 scopus 로고    scopus 로고
    • Effect of topical tazarotene in the treatment of congenital ichthyoses
    • Hofmann B, Stege H, Ruzicka T, et al. Effect of topical tazarotene in the treatment of congenital ichthyoses. Br J Dermatol 1999; 141: 642-646
    • (1999) Br J Dermatol , vol.141 , pp. 642-646
    • Hofmann, B.1    Stege, H.2    Ruzicka, T.3
  • 63
    • 35248854984 scopus 로고    scopus 로고
    • Treatment of ichthyosiform diseases with topically applied tazarotene: Risk of systemic absorption
    • Nguyen V, Cunningham BB, Eichenfield LF, et al. Treatment of ichthyosiform diseases with topically applied tazarotene: risk of systemic absorption. J Am Acad Dermatol 2007; 57 (5 Suppl.): S123-5
    • (2007) J Am Acad Dermatol , vol.57 , Issue.5 SUPPL.
    • Nguyen, V.1    Cunningham, B.B.2    Eichenfield, L.F.3
  • 64
    • 23444436515 scopus 로고    scopus 로고
    • Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene
    • Cotellessa C, Cuevas-Covarrubias SA, Valeri P, et al. Topical tazarotene 0.05% versus glycolic acid 70% treatment in X-linked ichthyosis due to extensive deletion of the STS gene. Acta Derm Venereol 2005; 85: 346-348
    • (2005) Acta Derm Venereol , vol.85 , pp. 346-348
    • Cotellessa, C.1    Cuevas-Covarrubias, S.A.2    Valeri, P.3
  • 65
    • 0036637153 scopus 로고    scopus 로고
    • Neonatal salicylate poisoning during the treatment of a collodion baby
    • Yamamura S, Kinoshita Y, Kitamura N, et al. Neonatal salicylate poisoning during the treatment of a collodion baby. Clin Pediatr (Phila) 2002; 41: 451-452
    • (2002) Clin Pediatr (Phila) , vol.41 , pp. 451-452
    • Yamamura, S.1    Kinoshita, Y.2    Kitamura, N.3
  • 66
    • 0034758164 scopus 로고    scopus 로고
    • Successful treatment of harlequin ichthyosis with acitretin
    • Singh S, Bhura M, Maheshwari A, et al. Successful treatment of harlequin ichthyosis with acitretin. Int J Dermatol 2001; 40: 472-473
    • (2001) Int J Dermatol , vol.40 , pp. 472-473
    • Singh, S.1    Bhura, M.2    Maheshwari, A.3
  • 67
    • 0021846718 scopus 로고
    • Harlequin fetus successfully treated with etretinate
    • Lawlor F, Peiris S. Harlequin fetus successfully treated with etretinate. Br J Dermatol 1985; 112: 585-590 (Pubitemid 15060999)
    • (1985) British Journal of Dermatology , vol.112 , Issue.5 , pp. 585-590
    • Lawlor, F.1    Peiris, S.2
  • 68
    • 0030621544 scopus 로고    scopus 로고
    • A retrospective study on 16 collodion babies
    • Ozturk A, Caksen H, Cetin N, et al. A retrospective study on 16 collodion babies. Turk J Pediatr 1997; 39: 55-59
    • (1997) Turk J Pediatr , vol.39 , pp. 55-59
    • Ozturk, A.1    Caksen, H.2    Cetin, N.3
  • 69
    • 33747339417 scopus 로고    scopus 로고
    • Serine protease signaling of epidermal permeability barrier homeostasis
    • Hachem JP, Houben E, Crumrine D, et al. Serine protease signaling of epidermal permeability barrier homeostasis. J Invest Dermatol 2006; 126: 2074-2086
    • (2006) J Invest Dermatol , vol.126 , pp. 2074-2086
    • Hachem, J.P.1    Houben, E.2    Crumrine, D.3
  • 70
    • 49649110726 scopus 로고    scopus 로고
    • Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosis
    • Haenssle HA, Finkenrath A, Hausser I, et al. Effective treatment of severe thermodysregulation by oral retinoids in a patient with recessive congenital lamellar ichthyosis. Clin Exp Dermatol 2008; 33 (5): 578-581
    • (2008) Clin Exp Dermatol , vol.33 , Issue.5 , pp. 578-581
    • Haenssle, H.A.1    Finkenrath, A.2    Hausser, I.3
  • 71
    • 27544501788 scopus 로고    scopus 로고
    • Topical pimecrolimus: A novel therapeutic option for Netherton syndrome
    • Oji V, Beljan G, Beier K, et al. Topical pimecrolimus: a novel therapeutic option for Netherton syndrome. Br J Dermatol 2005; 153: 1067-1068
    • (2005) Br J Dermatol , vol.153 , pp. 1067-1068
    • Oji, V.1    Beljan, G.2    Beier, K.3
  • 72
    • 0034978116 scopus 로고    scopus 로고
    • Significant absorption of topical tacrolimus in 3 patients with Netherton syndrome
    • Allen A, Siegfried E, Silverman R, et al. Significant absorption of topical tacrolimus in 3 patients with Netherton syndrome. Arch Dermatol 2001; 137: 747-750
    • (2001) Arch Dermatol , vol.137 , pp. 747-750
    • Allen, A.1    Siegfried, E.2    Silverman, R.3
  • 73
    • 0029955227 scopus 로고    scopus 로고
    • An appraisal of acitretin therapy in children with inherited disorders of keratinization
    • Lacour M, Mehta-Nikhar B, Atherton DJ, et al. An appraisal of acitretin therapy in children with inherited disorders of keratinization. Br J Dermatol 1996; 134: 1023-1029
    • (1996) Br J Dermatol , vol.134 , pp. 1023-1029
    • Lacour, M.1    Mehta-Nikhar, B.2    Atherton, D.J.3
  • 74
    • 0026000188 scopus 로고
    • Ichthyosis bullosa of Siemens responds well to low-dosage oral retinoids
    • Steijlen PM, Van Dooren-Greebe RJ, Happle R, et al. Ichthyosis bullosa of Siemens responds well to low-dosage oral retinoids. Br J Dermatol 1991; 125: 469-471
    • (1991) Br J Dermatol , vol.125 , pp. 469-471
    • Steijlen, P.M.1    Van Dooren-Greebe, R.J.2    Happle, R.3
  • 75
    • 0034524721 scopus 로고    scopus 로고
    • Treatment of psoriasis with oral liarozole: A dose-ranging study
    • Berth-Jones J, Todd G, Hutchinson PE, et al. Treatment of psoriasis with oral liarozole: a dose-ranging study. Br J Dermatol 2000; 143: 1170-1176
    • (2000) Br J Dermatol , vol.143 , pp. 1170-1176
    • Berth-Jones, J.1    Todd, G.2    Hutchinson, P.E.3
  • 76
    • 33847031771 scopus 로고    scopus 로고
    • DNA-based prenatal diagnosis of harlequin ichthyosis and characterization of ABCA12 mutation consequences
    • Akiyama M, Titeux M, Sakai K, et al. DNA-based prenatal diagnosis of harlequin ichthyosis and characterization of ABCA12 mutation consequences. J Invest Dermatol 2007; 127: 568-573
    • (2007) J Invest Dermatol , vol.127 , pp. 568-573
    • Akiyama, M.1    Titeux, M.2    Sakai, K.3
  • 77
    • 0036191743 scopus 로고    scopus 로고
    • Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis
    • Bitoun E, Bodemer C, Amiel J, et al. Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis. Prenat Diagn 2002; 22: 121-126
    • (2002) Prenat Diagn , vol.22 , pp. 121-126
    • Bitoun, E.1    Bodemer, C.2    Amiel, J.3
  • 78
    • 0031849439 scopus 로고    scopus 로고
    • Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis
    • Rothnagel JA, Lin MT, Longley MA, et al. Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis. Prenat Diagn 1998; 18: 826-830
    • (1998) Prenat Diagn , vol.18 , pp. 826-830
    • Rothnagel, J.A.1    Lin, M.T.2    Longley, M.A.3
  • 79
    • 33644927003 scopus 로고    scopus 로고
    • Prenatal diagnosis for severe inherited skin disorders: 25 years' experience
    • Fassihi H, Eady RA, Mellerio JE, et al. Prenatal diagnosis for severe inherited skin disorders: 25 years' experience. Br J Dermatol 2006; 154: 106-113
    • (2006) Br J Dermatol , vol.154 , pp. 106-113
    • Fassihi, H.1    Eady, R.A.2    Mellerio, J.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.