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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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Bibliografski detalji
Glavni autori: Frainer, Renata Hubner, de Abreu, Luciana Boff, Pinto, Giselle Martins, de Carvalho, André Vicente Esteves, Meneghello, Luana Pizarro
Format: Artigo
Jezik:Inglês
Izdano: Sociedade Brasileira de Dermatologia 2013
Teme:
Online pristup: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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