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Encephalocraniocutaneous lipomatosis with calvarial exostosis - Case report and review of literature
Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland syndrome, is a rare syndrome with unknown etiology. The syndrome is characterized by a triad of unique cutaneous, ocular, and central nervous system (CNS) manifestations. The cutaneous hallmark, nevus psiloliparus (NP), along with...
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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/PMC3932575/ https://ncbi.nlm.nih.gov/pubmed/24604937 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-3026.125607 |
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