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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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Bibliografiske detaljer
Udgivet i:Case Rep Ophthalmol Med
Main Authors: Shrestha, U. D., Adhikari, S.
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi Publishing Corporation 2015
Fag:
Online adgang: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
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