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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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| Udgivet i: | Ther Adv Ophthalmol |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6311540/ https://ncbi.nlm.nih.gov/pubmed/30627696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2515841418817486 |
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