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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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| Publicado no: | Pan Afr Med J |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The African Field Epidemiology Network
2015
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| Assuntos: | |
| Acesso em linha: | 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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