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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Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2010
Matèries:
Case report
Accés en línia: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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