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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...
保存先:
| 出版年: | Case Rep Ophthalmol Med |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi Publishing Corporation
2015
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| 主題: | |
| オンライン･アクセス: | 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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