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Expanding the Genotypic Spectrum of Bathing Suit Ichthyosis
Author(s) -
Nareh V. Marukian,
Rong-hua Hu,
Brittany G. Craiglow,
Leonard M. Milstone,
Jing Zhou,
Amy Theos,
Hande Kaymakçalan,
Ayşe Deniz Akkaya,
Jouni J. Uitto,
Hassan Vahidnezhad,
Leila Youssefian,
Susan J. Bayliss,
Amy S. Paller,
Lynn M. Boyden,
Keith A. Choate
Publication year - 2017
Publication title -
jama dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.128
H-Index - 166
eISSN - 2168-6084
pISSN - 2168-6068
DOI - 10.1001/jamadermatol.2017.0202
Subject(s) - ichthyosis , congenital ichthyosis , compound heterozygosity , proband , medicine , genotype , missense mutation , genetics , pediatrics , mutation , dermatology , biology , gene
Bathing suit ichthyosis (BSI) is a rare congenital disorder of keratinization characterized by restriction of scale to sites of relatively higher temperature such as the trunk, with cooler areas remaining unaffected. Fewer than 40 cases have been reported in the literature. Bathing suit ichthyosis is caused by recessive, temperature-sensitive mutations in the transglutaminase-1 gene (TGM1). Clear genotype-phenotype correlations have been difficult to establish because several of the same TGM1 mutations have been reported in BSI and other forms of congenital ichthyosis. We identify novel and recurrent mutations in 16 participants with BSI.

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