Carney complex is a rare genetic disorder characterized by an increased risk for certain tumors to grow in different part of the body. People with Carney complex often have freckle-like spots on their skin and noncancerous tumors on different organs and parts of their body. Depending on their location, these tumors can lead to symptoms such as weak bones and muscles and hormone imbalances.
General Information
Carney complex is a rare genetic disorder that increases the risk of noncancerous tumors growing in different areas of the body.
In addition to having freckle-like skin spots, people with Carney complex can have very different symptoms depending on the location(s) of their tumors.
Carney complex is caused by a mutation in a specific gene or genes. It can be inherited (passed from parent to child), or it can occur randomly.
Healthcare providers look for several signs and symptoms to diagnose Carney complex, including freckle-like skin spots and tumors in different parts of the body.
Effective treatments, such as medication and surgery, can help address symptoms of Carney complex that are caused by tumors.
Research
NICHD conducts research on Carney complex and on disorders associated with it.
Find a Study
NICHD conducts several clinical research projects related to Carney complex.
More Information
Find answers to other common questions about Carney complex, such as its effects on fertility and whether it can be diagnosed before birth.
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