Number of the records: 1
Carneyho komplex
Record number d056733 Date 06.06.2025 Type M - MESH Topical term Carneyho komplex Other term English (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
UDC C04.557.450.565.550.312C04.588.894.309.500C14.280.459.500C16.131.077.229C16.131.831.108 Note Autosomal 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