Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports

INTRODUCTION: Mal de Meleda is a rare form of palmoplantar keratoderma, with autosomal recessive transmission. It is characterized by diffuse erythema and hyperkeratosis of the palms and soles. Recently, mutations in the ARS (component B) gene (ARS, MIM: 606119) on chromosome 8q24.3 have been identi...

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Detalhes bibliográficos
Main Authors: Bchetnia, Mbarka, Merdassi, Ahlem, Charfeddine, Cherine, Mgaieth, Fatma, Kassar, Selma, Ouechtati, Farah, Chouchene, Ibtissem, Boussen, Hamouda, Mokni, Mourad, Osman, Amel Dhahri-Ben, Boubaker, Med Samir, Abdelhak, Sonia, Elmatri, Leila
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2010
Assuntos:
Case report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2874570/
https://ncbi.nlm.nih.gov/pubmed/20406438
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-4-108
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