Encephalocraniocutaneous lipomatosis

Encephalocraniocutaneous lipomatosis (ECCL), is a rare condition primarily affecting the brain, eyes, and skin of the head and face.[2] It is characterized by unilateral subcutaneous and intracranial lipomas, alopecia, unilateral porencephalic cysts, epibulbar choristoma and other ophthalmic abnormalities. This condition is described as sporadic because it occurs in people without a history of the disorder in their family.[3]

Encephalocraniocutaneous lipomatosis
Other namesHaberland syndrome,[1]
SpecialtyNeurology

It was named after Haberland and Perou who first described it.[4]

Signs and Symptoms

Eighty to ninety percent of those with encephalocraniocutaneous lipomatosis are unable to produce and keep fat tissue and have multiple lipomas.[5] Other types of growths, including jaw tumours, may also occur.

Approximately two thirds of individuals with Encephalocraniocutaneous lipomatosis have intracranial and/or intraspinal lipomas. They also have an increased risk of developing a form of brain cancer known as a glioma. Other neurological issues that can occur include seizures, spasticity and variable intellectual disability. However, approximately one third of effected individuals have typical intelligence.

The most common ocular abnormality in encephalocraniocutaneous lipomatosis is a form of benign growth called a choristoma which can occur in one or both eyes. These may effect vision.[6] Other ocular symptoms include abnormally small eyes, small pupils, iris hypoplasia, sclerocornea, hypertrophic conjunctivae, an absent macular reflex and anterior chamber anomalies. There may be eyelid colobomas and short or abnormal palpebral fissures.[7] Skin tags often grow around the eyelids.[8]

Cause

Encephalocraniocutaneous lipomatosis can result from mutations in the FGFR1 gene, which provides instructions for making a protein called fibroblast growth factor receptor 1 (FGFR1). This receptor interacts with proteins called fibroblast growth factors (FGFs) to trigger signaling within cells. Signaling via the FGFR1 protein is involved in many critical processes, such as cell division and the regulation of cell growth and maturation. This signaling is important for the normal development and growth of several parts of the body, including the brain. In some people with ECCL, no FGFR1 gene mutation has been identified, and the cause of the disease is unknown. Other genetic changes are under study as possible causes of this condition.[9]

History

This condition was first described in 1970.

See also

References
  1. Koishi, Giovanna Negrisoli; Yoshida, Mauricio; Alonso, Nivaldo; Matushita, Hamilton; Goldenberg, Dov (2008). "Encephalocraniocutaneous lipomatosis (haberland's syndrome): a case report of a neurocutaneous syndrome and a review of the literature". Clinics. 63 (3): 406–408. doi:10.1590/S1807-59322008000300020. PMC 2664244. PMID 18568254.
  2. Reference, Genetics Home. "ECCL". Genetics Home Reference. Retrieved 22 September 2017.
  3. "Encephalocraniocutaneous lipomatosis: MedlinePlus Genetics". medlineplus.gov. Retrieved 2022-11-27.
  4. Haberland, C; Perou, M (February 1970). "Encephalocraniocutaneous lipomatosis. A new example of ectomesodermal dysgenesis". Archives of Neurology. 22 (2): 144–55. doi:10.1001/archneur.1970.00480200050005. ISSN 0003-9942. PMID 4902772.
  5. "Encephalocraniocutaneous lipomatosis". National Organisation for Rare Disorders. Retrieved July 7, 2021.
  6. "Encephalocraniocutaneous lipomatosis". MedlinePlus. Retrieved July 7, 2021.
  7. "ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS;ECCL". Online Mendelian Inheritance in Man. Retrieved July 7, 2021.
  8. "Encephalocraniocutaneous lipomatosis". MedlinePlus. Retrieved July 7, 2021.
  9. "Encephalocraniocutaneous lipomatosis". 1 November 2016.


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