Cowden syndrome 4

Cowden syndrome 4 is a form of Cowden disease that occurs because of a mutation in the KLLN gene. This condition is one of several types of Cowden disease and is sometimes referred to by other names such as Cowden disease caused by mutation in KLLN, Cowden syndrome type 4, KLLN Cowden disease, or CWS4. People with this condition have a genetic alteration that sets it apart from other types of Cowden disease. Information about many aspects of the condition remains limited, but the key feature is the genetic cause linked to a mutation in the KLLN gene.

Information about symptoms is currently limited for this condition.

Cowden syndrome 4 is caused by a mutation in the KLLN gene. This genetic change is the key factor that leads to the development of this specific form of Cowden disease.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.