Similar Diseases
- ECCL
- Epidermal Nevus Syndrome
- Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
- Cerebellotrigeminal dermal dysplasia
- Cloves Syndrome
- Macrocephaly-capillary malformation
- Mulvihill-Smith syndrome
- Amyotrophy-fat tissue anomaly syndrome
- Cleft lip/palate-deafness-sacral lipoma syndrome
- Cutaneous hemangioma with muscle or bone atrophy
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Encephalocraniocutaneous lipomatosis – Abstract
Encephalocraniocutaneous lipomatosis (ECCL), otherwise known as Haberland syndrome, is a rare condition primarily affecting the brain, eyes, and skin of the head and face. It is characterized by unilateral subcutaneous and intracranial lipomas, alopecia, unilateral porencephalic cysts, epibulbar choristoma and other ophtalmic abnormalities.
It was named after Haberland and Perou who first described it.
Nevus psiloliparus – Abstract
Nevus psiloliparus is a cutaneous condition, a rare scalp anomaly characterized by a variable degree of alopecia and an excessive amount of adipose tissue.
It is the main hallmark of encephalocraniocutaneous lipomatosis (ECCL), otherwise known as Haberland syndrome.