Hypothyroidism in paediatric patients with Prader-Willi syndrome; regular monitoring is recommended

Hypothyroidism in paediatric patients with Prader-Willi syndrome; regular monitoring is recommended

Prader-Willi syndrome (PWS) is a genetic disorder described by multifaceted clinical features with implications on the endocrine system, metabolism, and behavior. Some symptoms of PWS syndrome can be confused with the relative clinical aspects of hypothyroidism, such as lethargy, muscular hypotonia,...

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Bibliographic Details
Main Authors: Hussain Alsaffar, Wasnaa Hadi Abdullah, Sawsan Ali Hussein
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Medical Journal of Babylon
Subjects:
growth hormone
hypothyroidism
prader-willi syndrome
thyroid function
Online Access:http://www.medjbabylon.org/article.asp?issn=1812-156X;year=2022;volume=19;issue=2;spage=123;epage=125;aulast=Alsaffar

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http://www.medjbabylon.org/article.asp?issn=1812-156X;year=2022;volume=19;issue=2;spage=123;epage=125;aulast=Alsaffar

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