Clinical Case A clinical case of Prader-Willi syndrome
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...
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Main Authors: | , , , , , |
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Format: | Book |
Published: |
LLC "MEDIAFORMAT",
2024-01-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |