Prader-Willi syndrome: an update on obesity and endocrine problems

Prader-Willi syndrome (PWS) is a rare complex genetic disorder that results from a lack of expression of the paternally inherited chromosome 15q11-q13. PWS is characterized by hypotonia and feeding difficulty in early infancy and development of morbid obesity aggravated by uncontrolled hyperphagia a...

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Detalles Bibliográficos
Autores principales: Kim, Su Jin, Cho, Sung Yoon, Jin, Dong-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Pediatric Endocrinology 2021
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749024/
https://www.ncbi.nlm.nih.gov/pubmed/34991300
http://dx.doi.org/10.6065/apem.2142164.082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749024/
https://www.ncbi.nlm.nih.gov/pubmed/34991300
http://dx.doi.org/10.6065/apem.2142164.082

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