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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Bibliographic Details
Published in:J Pediatr Genet
Main Authors: Toral-López, Jaime, Córdoba-Cabeza, Tania, Villeda, Maricela, Cortes-Castillo, Gabriel, Zenteno, Juan Carlos
Format: Artigo
Language:Inglês
Published: Georg Thieme Verlag KG 2013
Online Access: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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