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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...
Kaydedildi:
| Yayımlandı: | BMJ Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Publishing Group
2016
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| Konular: | |
| Online Erişim: | 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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