Kaufman Oculo-cerebro-facial Syndrome in a child with small and absent terminal phalanges and absent nails

BACKGROUND: Kaufman oculo-cerebro-facial syndrome (KOS) is caused by recessive UBE3B mutations and presents with microcephaly, ocular abnormalities, distinctive facial morphology, low cholesterol levels and intellectual disability. We describe a child with microcephaly, brachycephaly, hearing loss,...

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Detalles Bibliográficos
Autores principales: Kariminejad, Ariana, Ajeawung, Norbert Fonya, Bozorgmehr, Bita, Dionne-Laporte, Alexandre, Molidperee, Sirinart, Najafi, Kimia, Gibbs, Richard A, Lee, Brendan H, Hennekam, Raoul C, Campeau, Philippe M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370204/
https://www.ncbi.nlm.nih.gov/pubmed/28003643
http://dx.doi.org/10.1038/jhg.2016.151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370204/
https://www.ncbi.nlm.nih.gov/pubmed/28003643
http://dx.doi.org/10.1038/jhg.2016.151

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