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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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Detalles Bibliográficos
Autores principales: Koti, Kalyan, Bhimireddy, Vijayalakshmi, Dandamudi, Srinivas, Gunnamreddy, Ramanareddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3667289/
https://www.ncbi.nlm.nih.gov/pubmed/23723477
http://dx.doi.org/10.4103/0019-5154.110835