{"id":12830,"date":"2024-09-08T12:47:18","date_gmt":"2024-09-08T10:47:18","guid":{"rendered":"https:\/\/valintermed.com\/?p=12830"},"modified":"2024-09-08T12:47:19","modified_gmt":"2024-09-08T10:47:19","slug":"sindrom-rotmunda-tomsona","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/rotmunda-tomsona-syndrome\/","title":{"rendered":"Rothmund-Thomson syndrome"},"content":{"rendered":"
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Rothmund-Thomson syndrome (RT) is a rare genetic disorder that causes a variety of symptoms involving the skin, eyes, and skeletal system. The main characteristics of the syndrome include a predisposition to neoplasms, especially basal cell carcinoma, and various abnormalities in appearance, such as hypopigmentation and hair growth abnormalities. Patients with RT syndrome may also have distinctive facial features, including wide cheekbones and a flat nose. In addition to the systems mentioned above, patients may have endocrine system disorders and functional disorders of internal organs. The nature of Rothmund-Thomson syndrome lies in genetic mutations, which makes it an interesting object for research into the interactions between genetics and phenotype.<\/p>\n

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