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Encephalocraniocutaneous lipomatosis (Haberland syndrome): A rare case report
Haberland syndrome or Fishman syndrome also known as encephalocraniocutaneous lipomatosis (ECCL) is a rare, congenital neurocutaneous disorder. It is characterized by unilateral involvement of skin, eyes and central nervous system. We report the case of a 28-year-old woman who presented with soft li...
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| Yayımlandı: | Indian Dermatol Online J |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Medknow Publications & Media Pvt Ltd
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5134170/ https://ncbi.nlm.nih.gov/pubmed/27990391 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.193901 |
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