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Encephalocraniocutaneous Lipomatosis (Haberl and syndrome): A Case Report and Review of Literature
Encephalocraniocutaneous lipomatosis (ECCL) is a rare sporadic neurocutaneous syndrome characterized by presence of central nervous system, ocular and cutaneous anomalies. The exact pathogenesis is still not known. We present the third case from the Indian subcontinent, who is a five year old girl w...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3667289/ https://ncbi.nlm.nih.gov/pubmed/23723477 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.110835 |
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