Familial atypical multiple mole melanoma syndrome

Introduction: Familial atypical multiple mole melanoma syndrome

Description of Familial atypical multiple mole melanoma syndrome

Familial atypical multiple mole melanoma syndrome: FAMMM syndrome. An inherited condition marked by the following: (1) one or more first- or second-degree relatives (parent, sibling, child, grandparent, grandchild, aunt, or uncle) with malignant melanoma; (2) many moles, some of which are atypical (asymmetrical, raised, and/or different shades of tan, brown, black, or red) and often of different sizes; and (3) moles that have specific features when examined under a microscope. FAMMM syndrome increases the risk of melanoma and may increase the risk of pancreatic cancer.
Source: National Institute of Health

Familial atypical multiple mole melanoma syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial atypical multiple mole melanoma syndrome:

• Familial
• Familial disorder
• Atypical
• Mole
• Mole symptoms (29 causes)
• Melanoma
• FAMMM
• Inherited
• Inherited disease
• Inherited disorder

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