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PTEN Hamartoma Tumor Syndrome: PTEN Hamartoma Tumor Syndrome is a group of conditions caused by a mutation in the PTEN gene. The primary characteristic of the condition is the development of multiple hamartomas (tumor-like growth) in virtually any part of the body. The growths are generally not cancerous but patients often have an increased risk of developing various cancers. Specific conditions covered by this term are Cowden syndrome, BAnnayan-Riley-Ruvalcaba Syndrome and Proteus syndrome. More detailed information about the symptoms, causes, and treatments of PTEN Hamartoma Tumor Syndrome is available below.
See full list of 15 symptoms of PTEN Hamartoma Tumor Syndrome
Review possible medical complications related to PTEN Hamartoma Tumor Syndrome:
See full list of 11 treatments for PTEN Hamartoma Tumor Syndrome
Prognosis for PTEN Hamartoma Tumor Syndrome: The prognosis is variable depending on the individual case. Prognosis can be improved by closely monitoring for the development of cancer.
More about prognosis of PTEN Hamartoma Tumor Syndrome
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