Encephalocraniocutaneous lipomatosis (ECCL): differential diagnosis
Evidence-based neurology checklist on encephalocraniocutaneous lipomatosis (eccl): differential diagnosis: Differential diagnosis of ECCL Nevus sebaceous syndrome Proteus syndrome Sturge-Weber syndrome Neurofibromatosis type 1 (NF1) Oculoectodermal syndrome Oculo-auriculo-vertebral syndrome…
Differential diagnosis of ECCL
- Nevus sebaceous syndrome
- Proteus syndrome
- Sturge-Weber syndrome
- Neurofibromatosis type 1 (NF1)
- Oculoectodermal syndrome
- Oculo-auriculo-vertebral syndrome (Goldenhar syndrome)
- Culocerebrocutaneous syndrome (Delleman-Oorthuys syndrome)
- Focal dermal hypoplasia syndrome (Gorlin-Goltz syndrome)
- Epidermal nevus syndrome (Schimmelpenning syndrome)
Synonyms
References
- Chandravanshi SL. Encephalocraniocutaneous lipomatosis: a case report and review of the literature. Indian J Ophthalmol 2014; 62:622-627.
- Rubegni P, Risulo M, Sbano P, Buonocore G, Perrone S, Fimiani M. Encephalocraniocutaneous lipomatosis (Haberland syndrome) with bilateral cutaneous and visceral involvement. Clin Exp Dermatol 2003; 28:387-390.