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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...

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Detalhes bibliográficos
Publicado no:BMJ Case Rep
Main Authors: Ribeiro, Bárbara, Igreja, Joana, Gonçalves-Rocha, Miguel, Cadilhe, Alexandra
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2016
Assuntos:
Acesso em linha: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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