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Somatic Mosaicism for a “Lethal” GJB 2 Mutation Results in a Patterned Form of Spiny Hyperkeratosis without Eccrine Involvement
Author(s) -
EskinSchwartz Marina,
Metzger Yoav,
Peled Alon,
WeissglasVolkov Daphna,
Malchin Natalia,
Gat Andrea,
Vodo Dan,
Mevorah Baruch,
Shomron Noam,
Sprecher Eli,
Sarig Ofer
Publication year - 2016
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/pde.12848
Subject(s) - hyperkeratosis , epidermolytic hyperkeratosis , context (archaeology) , mutation , genetics , exome sequencing , germline mutation , biology , medicine , dermatology , pathology , gene , paleontology
Background Spiny hyperkeratosis refers to a rare clinical phenotype characterized by nonfollicular keratotic projections and sometimes associated with other acquired and inherited conditions. We describe a case of congenital patterned spiny hyperkeratosis. Methods To identify the cause of this disorder, we used a combination of whole exome sequencing, direct sequencing and TaqMan assay. Results We found that the peculiar clinical features displayed by the patient are due to somatic mosaicism for a heterozygous mutation in the GJB2 gene. Conclusion Because histopathologic examination of two independent biopsies did not reveal porokeratotic eccrine ostial and dermal duct nevus (PEODDN), previously reported to result from somatic mutations in GJB2 , it appears that mutations in this gene can cause nevoid spiny hyperkeratosis in the context of PEODDN or as an isolated finding.