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Cerebral hemihypoplasia and nevus flammeus in a child with oromandibular limb hypogenesis syndrome type III
Oromandibular limb hypogenesis syndrome (OMLH; OMIM 103300) encompasses a group of uncommon disorders characterized by malformations in the mouth, jaw and limbs. It has been associated with various entities such as gastroschisis, pulmonary hypoplasia, intestinal atresia, renal agenesis, hydrocephalu...
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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
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5020958/ https://ncbi.nlm.nih.gov/pubmed/27625839 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-13047 |
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