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Delleman–Oorthuys syndrome (oculocerebrocutaneous syndrome) in a Nigerian child: a case report

BACKGROUND: Delleman–Oorthuys syndrome, also known as oculocerebrocutaneous syndrome, is a rare congenital anomaly with ocular, cerebral and cutaneous manifestations. So far, only 40 cases have been described. CLINICAL CASE: A 3-year-old female Nigerian child with no identifiable left eyeball, multi...

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Detalles Bibliográficos
Autores principales:	Badejo, Oluwakemi A., Fasina, Oluyemi, Balogun, James A., Ogunbiyi, John O., Shokunbi, Matthew T.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2018
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6311540/ https://www.ncbi.nlm.nih.gov/pubmed/30627696 http://dx.doi.org/10.1177/2515841418817486

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