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    SubjectsDermatologyFamilial Atypical Mole Melanoma Syndrome
    ClinicalDermatology

    Familial Atypical Mole Melanoma Syndrome

    1 MCQs in Dermatology for NEET PG

    1 Medium
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    Sample Questions

    medium

    A 35-year-old woman presents to dermatology with a history of multiple atypical moles and a family history of melanoma in her mother and maternal grandmother. Genetic testing reveals a germline mutation in the gene marked **A** (CDKN2A 9p21). Which of the following best explains the mechanism by which loss of function of this gene increases melanoma susceptibility?

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