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Occurrence of Synpolydactyly and Omphalocele in a Fetus with a HOXD13 Mutation
Synpolydactyly (SPD) is an autosomal dominant congenital limb disorder due to mutations in HOXD13 . It is a phenotypically heterogeneous condition characterized by syndactyly of the third finger (F3), fourth finger (F4) and/or fourth toe (T4), and fifth toe (T5) with variably associated polydactyly....
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| Publicado no: | J Pediatr Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Georg Thieme Verlag KG
2017
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5548533/ https://ncbi.nlm.nih.gov/pubmed/28794915 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0037-1602142 |
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