Early Diagnosis in Prader–Willi Syndrome Reduces Obesity and Associated Co-Morbidities

Prader–Willi syndrome (PWS) is an imprinting genetic disorder characterized by lack of expression of genes on the paternal chromosome 15q11–q13 region. Growth hormone (GH) replacement positively influences stature and body composition in PWS. Our hypothesis was that early diagnosis delays onset of o...

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Détails bibliographiques
Publié dans:Genes (Basel)
Auteurs principaux: Kimonis, Virginia E., Tamura, Roy, Gold, June-Anne, Patel, Nidhi, Surampalli, Abhilasha, Manazir, Javeria, Miller, Jennifer L., Roof, Elizabeth, Dykens, Elisabeth, Butler, Merlin G., Driscoll, Daniel J.
Format: Artigo
Langue:Inglês
Publié: MDPI 2019
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6896038/
https://ncbi.nlm.nih.gov/pubmed/31698873
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10110898
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