Pallister–Hall syndrome with orofacial narrowing and tethered cord: a case report

BACKGROUND: Pallister–Hall syndrome is a rare, autosomal dominant, genetic disorder characterized by different congenital abnormalities: hypothalamic hamartoblastoma, bifid or shortened epiglottis, polydactyly, renal anomalies, and imperforate anus. CASE PRESENTATION: In this case report, we describ...

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Detalles Bibliográficos
Autor principal: Hayek, Femia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262955/
https://www.ncbi.nlm.nih.gov/pubmed/30486853
http://dx.doi.org/10.1186/s13256-018-1868-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262955/
https://www.ncbi.nlm.nih.gov/pubmed/30486853
http://dx.doi.org/10.1186/s13256-018-1868-8

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