Article
Carney complex: a curious case of a rare cancer syndrome caused by a novel pathogenic mutation in the PRKAR1A gene.
BMJ case reports - 13 Apr 2021
Gupta Nisha, Kitzler Thomas, Albrecht Steffen, Larouche Vincent
Abstract excerpt
A 39-year-old woman was referred to the cancer genetics outpatient clinic for a clinical diagnosis of Carney complex (CNC) in her deceased brother. The patient had some characteristic clinical features such as periorbital lentigines and coarse facial features, suggestive of CNC; however, she did not meet major diagnostic criteria for CNC. Previous extensive investigations revealed a mild insulin-like growth...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
