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"Nails Only" Phenotype and Partial Dominance of p.Glu170Lys Mutation in a Family with Epidermolysis Bullosa Simplex.
González-Cantero, Álvaro; Sánchez-Moya, Ana Isabel; Pérez-Hortet, Cristina; Martínez-Lorenzo, Elena; Gómez-Dorado, Blas; Schoendorff-Ortega, Cristina.
Afiliação
  • González-Cantero Á; Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain.
  • Sánchez-Moya AI; Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain.
  • Pérez-Hortet C; Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain.
  • Martínez-Lorenzo E; Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain.
  • Gómez-Dorado B; Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain.
  • Schoendorff-Ortega C; Department of Dermatology, Complejo Hospitalario de Toledo, Toledo, Spain.
Pediatr Dermatol ; 34(4): e205-e206, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28425111
Epidermolysis bullosa (EB) is a heterogeneous group of rare, chronic, inherited skin disorders characterized by marked mechanical fragility of epithelial tissues, with blistering and erosions after minor trauma. We present the first report of a nails-only phenotype in two patients with epidermolysis bullosa simplex (EBS) and a heterozygous pGlu170Lys mutation and the second reported case of EBS associated with a homozygous p.Glu170Lys mutation in the KRT5 gene. Our findings may be relevant for genetic counseling and for understanding the inheritance pattern of EBS.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epidermólise Bolhosa Simples / Queratina-5 / Unhas Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epidermólise Bolhosa Simples / Queratina-5 / Unhas Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article