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...

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Detalles Bibliográficos
Autores principales: Shrestha, U. D., Adhikari, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617704/
https://www.ncbi.nlm.nih.gov/pubmed/26635984
http://dx.doi.org/10.1155/2015/435967

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617704/
https://www.ncbi.nlm.nih.gov/pubmed/26635984
http://dx.doi.org/10.1155/2015/435967

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