Do you know this syndrome?()

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Frainer, Renata Hubner, de Abreu, Luciana Boff, Pinto, Giselle Martins, de Carvalho, André Vicente Esteves, Meneghello, Luana Pizarro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2013
Materias:
Syndrome In Question
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699942/
https://www.ncbi.nlm.nih.gov/pubmed/23539021
http://dx.doi.org/10.1590/S0365-05962013000100023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699942/
https://www.ncbi.nlm.nih.gov/pubmed/23539021
http://dx.doi.org/10.1590/S0365-05962013000100023

Ejemplares similares