Encephalo-Cranio-cutaneous lipomatosis [ECCL] with cardiac affection case report

Neurocutaneous syndromes are numbers of diseases characterized by collection of neurological and cutaneous manifestations. ECCL is a rare, congenital, neurocutaneous disorder characterized by associated opthalmological affection, first described in 1970 by Haberland and Perou. We reported 4.5 years male child demonstrated the main features of ECCL; cutaneous and neurological manifestations with opthalmological features in the form of conjunctival and corneal dermoids. Some cardiac anomalies were also observed in our patient which were not reported before