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

Internet

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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