Syndromic anorectal malformation associated with Holt–Oram syndrome, microcephaly, and bilateral corneal opacity: a case report

BACKGROUND: The occurrence of an anorectal malformation with Holt–Oram syndrome, microcephaly, and bilateral corneal opacity is rare and to the best of our knowledge has not previously been reported in the literature. Hence, there is a need to document our experience in this case and learn as much a...

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Detalles Bibliográficos
Autores principales: Usang, Usang E., Agan, Thomas U., Inyang, Akan W., Emehute, John-Daniel C., Itam, Itam H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974687/
https://www.ncbi.nlm.nih.gov/pubmed/27495810
http://dx.doi.org/10.1186/s13256-016-1011-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974687/
https://www.ncbi.nlm.nih.gov/pubmed/27495810
http://dx.doi.org/10.1186/s13256-016-1011-7

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