Encephalocraniocutaneous lipomatosis (Haberland 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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Format: | Book |
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Wolters Kluwer Medknow Publications,
2013-01-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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Copy 1 | Available |