{"id":12690,"date":"2024-10-11T17:21:00","date_gmt":"2024-10-11T15:21:00","guid":{"rendered":"https:\/\/valintermed.com\/?p=12690"},"modified":"2024-10-11T17:21:00","modified_gmt":"2024-10-11T15:21:00","slug":"sindrom-opuholi-gamartomy-pten","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/tumour-gamartomy-syndrome\/","title":{"rendered":"PTEN hamartoma tumor syndrome"},"content":{"rendered":"
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PTEN hamartoma tumor syndrome (PH-PTEN) is a hereditary disorder that belongs to a group of syndromes associated with a predisposition to tumor formation. This condition is associated with abnormalities in the PTEN gene, which plays a key role in the regulation of cell growth and apoptosis. The main manifestations of the syndrome are the formation of hamartomas - benign tumors affecting various organs and systems. Patients with PH-PTEN are at high risk of developing various malignancies, including breast, thyroid, and endometrial cancer. In addition, the syndrome may be accompanied by neurological disorders, skin manifestations, and multiple other systemic disorders.<\/p>\n

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