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...

Full description

Saved in:
Bibliographic Details
Main Authors: Aleksandra V. Serezhkina (Author), Irina G. Khmelevskaya (Author), Natalia S. Razinkova (Author), Darya R. Yakovleva (Author), Tatiana A. Minenkova (Author), Rostislav E. Gromov (Author)
Format: Book
Published: LLC "MEDIAFORMAT", 2024-01-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available