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Original Query
What is cancer familial atypical multiple mole melanoma syndrome?
Search Results
- cancer familial atypical multiple mole melanoma syndrome
Preview- It really is clear that, risk of developing pancreatic cancer in families with familial atypical multiple mole malignant melanoma associated with a specific nineteen deletion of p16 (p16-Leiden). Pancreatic cancer is a disease in which malignant (cancer) cells are found in the tissues of the pancreas. Also called exocrine (i.e., eccrine) cancer.
- It could seem apparant that, similarly, people with hereditary dysplastic nevus (i.e., dysplastic nevus syndrome (i.e., dysplastic nevus)) syndrome or familial atypical multiple mole melanoma (FAMMM) syndrome are also at increased risk for developing melanoma. Hereditary, transmitted from parent to child by information contained in the genes. Nevus is a benign (not cancer) growth on the skin that is formed by a cluster of melanocytes (cells that make a substance called melanin, which gives color to skin and eyes). A nevus is usually dark and may be raised from the skin. Also called mole.
- It`s obvious that, phenotypic variation (i.e., type) in eight extended CDKN2.
