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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Bibliografiska uppgifter
I publikationen:Pan Afr Med J
Huvudupphovsmän: Hbibi, Mohamed, Abourazzak, Sana, Idrissi, Mounia, Chaouki, Sana, Atmani, Samir, Hida, Moustapha
Materialtyp: Artigo
Språk:Inglês
Publicerad: The African Field Epidemiology Network 2015
Ämnen:
Case Report
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4430157/
https://ncbi.nlm.nih.gov/pubmed/25995800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2015.20.3.5878
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