Carney complex, type 1

Carney complex, type 1 is a rare condition that is defined by the presence of a mutation in the PRKAR1A gene. This mutation leads to the development of features that may involve multiple body systems. The condition is sometimes referred to by other names such as Carney complex caused by mutation in PRKAR1A, Carney syndrome, and other related names, which reflects its varied clinical presentation.

Information about symptoms is currently limited for this condition.

Carney complex, type 1 is caused by a mutation in the PRKAR1A gene. This genetic change is the defining cause of the condition, although detailed information about other risk factors or the full range of genetic influences is limited.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition. Ongoing studies are looking into the effects of the PRKAR1A mutation and how to better understand and manage this rare complex condition.