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Carney syndrome is a rare autosomal dominant disorder that can cause HGH-secreting pituitary tumors and acromegaly in about 20% of patients who have the syndrome. Carney syndrome is associated with a defective gene on chromosome 2.
Carney Syndrome
LAMB - Lentigines, atrial myxoma, mucocutaneous myoma, blue nevus syndrome
NAME - Nevi, atrial myxoma, skin myxoma, ephelides syndrome
See How are genetic conditions and genes named? in the Handbook.
Carney syndrome
Carnitine Deficiency Secondary to MCAD Deficiency
Carnitine Deficiency Syndrome
Carnitine Deficiency, Myopathic
Carnitine Deficiency, Primary
Carnitine Deficiency, Secondary
Carnitine Palmitoyltransferase 1A Deficiency ...
Also called Carney syndrome.
Permalink for Carney complex
Carney dyad (KAR-nee DY-ad) A rare, inherited disorder marked by tumors of the gastrointestinal tract and tumors that form in embryonic nervous tissue in the head, neck, and torso.
 See also: Symptom, Arthritis, Cancer, Smoking, Copd
  
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