Familial atypical multiple mole melanoma syndrome

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Familial atypical multiple mole melanoma syndrome

Synonyms: B-K mole syndrome | FAMM-PC syndrome | FAMMM syndrome | Familial atypical mole syndrome | Familial atypical multiple mole melanoma-pancreatic carcinoma syndrome | Familial dysplastic nevus syndrome | Melanoma-pancreatic cancer syndrome

Familial atypical multiple mole melanoma (FAMMM) syndrome is an inherited genodermatosis characterized by the presence of multiple melanocytic nevi (often >50) and a family history of melanoma as well as in a subset of patients an increased risk of developing pancreatic cancer (see this term) and other malignancies.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version February 2024

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Familial atypical multiple mole melanoma syndrome?

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Clinical Trials

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