Establishing perinatal and neonatal features of Prader-Willi syndrome for efficient diagnosis and outcomes

Authors :: Lili Yang
Shujiong Mao
Bo Ma
Chaochun Zou
Qiong Zhou
Source :: Expert Opinion on Orphan Drugs. 8:265-271
Publication Year :: 2020
Publisher :: Informa UK Limited, 2020.
Abstract: Prader-Willi syndrome (PWS) is the most common genetic disease causing childhood morbid obesity. Early diagnosis and treatment are utmost important for improving prognosis and bettering outcome in ...

Subjects :: congenital, hereditary, and neonatal diseases and abnormalities
Pediatrics
medicine.medical_specialty
business.industry
Health Policy
nutritional and metabolic diseases
Disease
nervous system diseases
body regions
Morbid obesity
03 medical and health sciences
0302 clinical medicine
030220 oncology & carcinogenesis
Medicine
Pharmacology (medical)
business
Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
030217 neurology & neurosurgery

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