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May 29, 2023 · Muir-Torre syndrome is a rare genetic disorder that increases your risk of skin tumors and internal cancers, often colorectal cancer. Learn about the types, diagnosis, management and prevention of this condition.
Muir–Torre syndrome is a rare hereditary, autosomal dominant cancer syndrome: 663 that is thought to be a subtype of HNPCC (Lynch syndrome). Individuals are prone to develop cancers of the colon, genitourinary tract, and skin lesions, such as keratoacanthomas and sebaceous tumors .
Muir-Torre syndrome (MTS) is a form of Lynch syndrome and is characterized by sebaceous (oil gland) skin tumors in association with internal cancers.
Jul 3, 2023 · Muir-Torre Syndrome is an autosomal dominant disorder that is a phenotypic variant of hereditary non-polyposis colorectal cancer (HNPCC) which is also known as Lynch syndrome. It is caused by mutations in DNA mismatch repair genes which results in microsatellite instability.
Feb 16, 2023 · Muir-Torre syndrome (MTS) is a rare, inherited condition that causes tumors on the skin and in internal organs. Learn about the symptoms, causes, risk factors, diagnosis, treatment, and outlook for people with MTS.
Apr 20, 2015 · Muir-Torre syndrome is an inherited syndrome characterized by sebaceous neoplasms and visceral malignancies. A newly identified subtype of Muir-Torre syndrome displays microsatellite stability and autosomal recessive inheritance.
Lynch syndrome is an inherited syndrome that predisposes to cancer, including sebaceous tumours and keratoacanthomas. Muir-Torre syndrome is a rare variant of Lynch syndrome, mainly caused by MSH2 gene mutations.
