Cortes Lacassie syndrome

Cortes Lacassie syndrome is a rare disease that is characterized by seizures, abnormalities in nails, hair and teeth, and malformed hands and feet. It is named after Fanny Cortes and Yves Lacassie, two researchers from the University of Chile who discovered the disease in 1986.[1] Cortes Lacassie syndrome is considered a rare disease and has only been recorded in one case, leading to death at 31 months.[2]

Symptoms

This disease is characterized by agenesis of fingers and toes, and hypotrophy of fingernails at birth. At 3 months, the baby exhibited delayed psychomotor development and developed myoclonic seizures. Chromosomal study indicated no abnormalities. The baby developed acute epileptic seizures, acute renal failure, and hepatorenal syndrome, passing away at 31 months.[1]

Cortes Lacassie syndrome is a form of ectodermal dysplasia, postulated to be a new type of the group of tricho-odonto-onychic disorders.

References
  1. Cortes, Fanny; Lacassie, Yves; Fraser, F. Clarke; Preus, Marilyn (1986-10-01). "An unusal case of ectodermal dysplasia". American Journal of Medical Genetics. 25 (2): 289–291. doi:10.1002/ajmg.1320250213. ISSN 1096-8628. PMID 3777024.
  2. "Cortes Lacassie syndrome — CheckOrphan". www.checkorphan.org. Retrieved 2017-04-24.
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