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ORPHA:144· ICD-10 C18.2· Lynch syndrome

Визначення(English summary)

A rare form of hereditary nonpolyposis colon cancer (HNPCC) characterized by predisposition to a wide variety of cancers, including neoplasms of the digestive tract, urinary tract, endometrium, ovary, brain, and prostate, as well as sebaceous skin tumors. LS-associated tumors are typically characterized by the presence of microsatellite instability (MSI) and loss of expression of MMR proteins in tumor tissue.

Поширеність
Unknown
Успадкування
Autosomal dominant
Вік початку
Adult