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Carneyho komplex

  1. Subject h.Carneyho komplex
    Subject h.Carney Complex
    Entry termsCarneyho komplex, typ 2
    Carneyho komplex typu II
    Carneyho myxóm-endokrinný komplex
    Carneyov syndróm
    LAMB syndróm
    myxóm, pigmentové škvrny a zvýšená endokrinná aktivita
    NAME syndróm
    English X referencesCarney Complex, Type 2
    Carney Complex, Type II
    Carney Myxoma-Endocrine Complex
    Carney Syndrome
    LAMB Syndrome
    Myxoma, Spotty Pigmentation, and Endocrine Overactivity
    NAME Syndrome
    Scope note in EnglishAutosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2).
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