Lipomatosis encefalocraneocutánea: reporte de caso

Eye and appearance characteristics of encephalocraniocutaneous lipomatosis

“…ECCL is a rare neurocutaneous syndrome with unknown etiology and multiple sporadic differences in ethnicity, gender, and family history. Since Haberland [1] described this syndrome in 1970, more than 60 instances of related disorders have been published worldwide, mainly reported via pediatrics, and neurosurgery cases [2,3]. The main features of the syndrome include asymmetric skin damage to the head and neck, central nervous system abnormalities(CNS), ocular abnormalities, often bilaterally.…”