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Overlap between Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly and Fuhrmann's Syndromes in an Egyptian Female Infant
We report a rare congenital limb defect with combined features of both fibular aplasia, tibial campomelia, and oligosyndactyly (FATCO) and Fuhrmann's syndromes. A female newborn infant, born to nonconsanguineous Egyptian parents, presented with isolated abnormalities of the lower limbs comprisi...
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| Yayımlandı: | J Pediatr Genet |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Georg Thieme Verlag KG
2017
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| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5423804/ https://ncbi.nlm.nih.gov/pubmed/28497002 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0036-1597931 |
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