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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Frainer, Renata Hubner, de Abreu, Luciana Boff, Pinto, Giselle Martins, de Carvalho, André Vicente Esteves, Meneghello, Luana Pizarro
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Sociedade Brasileira de Dermatologia 2013
Gaiak:
Sarrera elektronikoa: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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