A carregar...

Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract

Craniofacial microsomia (CFM) includes a spectrum of malformations primarily involving structures derived from the first and second branchial arches. Patients with hemifacial microsomia and epibulbar dermoids are said to have Goldenhar syndrome (GHS). Four-month-old boy with whitish pupillary reflex...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Case Rep Ophthalmol Med
Main Authors: Shrestha, U. D., Adhikari, S.
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4617704/
https://ncbi.nlm.nih.gov/pubmed/26635984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/435967
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!