Clinical Case A clinical case of Prader-Willi syndrome

• المؤلفون الرئيسيون: Aleksandra V. Serezhkina (مؤلف), Irina G. Khmelevskaya (مؤلف), Natalia S. Razinkova (مؤلف), Darya R. Yakovleva (مؤلف), Tatiana A. Minenkova (مؤلف), Rostislav E. Gromov (مؤلف)
• التنسيق: كتاب
• منشور في: LLC "MEDIAFORMAT", 2024-01-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Relevance. Prader-Willi syndrome (SPW) is a rare genetic disease associated with a predominant legion of the nervous system with subsequent involvement of other systems. The main signs of the syndrome part childhood hypotension, hypogonadism with hypogenitalism, morbid obesity, and impaired cognitiv...