Cutis Laxa syndrome: a case report

Cutis laxa (CL) is a heterogeneous group of inherited and acquired connective tissue disorders characterized by a loose skin and variable systemic involvement (inguinal hernia, cardiopulmonary disease, and emphysema). Autosomal dominant, autosomal recessive and x-linked recessive patterns have been...

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Detalles Bibliográficos
Autores principales: Hbibi, Mohamed, Abourazzak, Sana, Idrissi, Mounia, Chaouki, Sana, Atmani, Samir, Hida, Moustapha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430157/
https://www.ncbi.nlm.nih.gov/pubmed/25995800
http://dx.doi.org/10.11604/pamj.2015.20.3.5878

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430157/
https://www.ncbi.nlm.nih.gov/pubmed/25995800
http://dx.doi.org/10.11604/pamj.2015.20.3.5878

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