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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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| Pubblicato in: | Case Rep Ophthalmol Med |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Hindawi Publishing Corporation
2015
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| Soggetti: | |
| Accesso online: | 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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