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Congenital hypotrichosis and Stargardt macular dystrophy are rare autosomal recessive disorder of unknown etiology respectively characterized by hair loss, macular degeneration and severe progressive vision reduction. There are few reports in the literature with this association. Studies show that t...

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Detalhes bibliográficos
Main Authors: Frainer, Renata Hubner, de Abreu, Luciana Boff, Pinto, Giselle Martins, de Carvalho, André Vicente Esteves, Meneghello, Luana Pizarro
Formato: Artigo
Idioma:Inglês
Publicado em: Sociedade Brasileira de Dermatologia 2013
Assuntos:
Syndrome In Question
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3699942/
https://ncbi.nlm.nih.gov/pubmed/23539021
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/S0365-05962013000100023
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