Related MeSH Hierarchy (5)
Diseases [C] » Neoplasms [C04] » Neoplasms by Histologic Type » Neoplasms, Connective and Soft Tissue » Neoplasms, Connective Tissue » Myxoma » Carney Complex
Diseases [C] » Neoplasms [C04] » Neoplasms by Site » Thoracic Neoplasms » Heart Neoplasms » Carney Complex
Diseases [C] » Cardiovascular Diseases [C14] » Heart Diseases » Heart Neoplasms » Carney Complex
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Carney Complex
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Carney Complex
Description
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). MeSH
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Phase 2 Indicated Drugs (1)
Organization Involved with Phase 2 Indications (2)
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