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Carneyho komplex

  1. Record numberd056733
    Date06.06.2025
    TypeM - MESH
    Topical termCarneyho komplex
    Other termEnglish (Pseudonym) Carney Complex, Type 2
    English (Pseudonym) Carney Complex, Type II
    English (Pseudonym) Carney Myxoma-Endocrine Complex
    English (Pseudonym) Carney Syndrome
    English (Pseudonym) LAMB Syndrome
    English (Pseudonym) Myxoma, Spotty Pigmentation, and Endocrine Overactivity
    English (Pseudonym) NAME Syndrome
    Slovak (Pseudonym) Carneyho komplex, typ 2
    Slovak (Pseudonym) Carneyho komplex typu II
    Slovak (Pseudonym) Carneyho myxóm-endokrinný komplex
    Slovak (Pseudonym) Carneyov syndróm
    Slovak (Pseudonym) LAMB syndróm
    Slovak (Pseudonym) myxóm, pigmentové škvrny a zvýšená endokrinná aktivita
    Slovak (Pseudonym) NAME syndróm
    UDCC04.557.450.565.550.312C04.588.894.309.500C14.280.459.500C16.131.077.229C16.131.831.108
    NoteAutosomal 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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Number of the records: 1  

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