Article
Carney complex: an update.
European journal of endocrinology - 1 Oct 2015
Correa Ricardo, Salpea Paraskevi, Stratakis Constantine A
Abstract excerpt
Carney complex (CNC) is a rare autosomal dominant syndrome, characterized by pigmented lesions of the skin and mucosa, cardiac, cutaneous and other myxomas and multiple endocrine tumors. The disease is caused by inactivating mutations or large deletions of the PRKAR1A gene located at 17q22-24 coding for the regulatory subunit type I alpha of protein kinase A (PKA) gene. Most recently, components of the complex...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
