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Goldenhar syndrome: a rare diagnosis with possible prenatal findings
Goldenhar syndrome is a rare congenital disease associated with hemifacial hypoplasia as well as ear and ocular defects. Sometimes it is also associated with vertebral and other bone defects, cardiac malformations and central nervous system anomalies. Its aetiology is not yet clarified in the litera...
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| Udgivet i: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Publishing Group
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4932337/ https://ncbi.nlm.nih.gov/pubmed/27329096 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2016-215258 |
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