Impact of genetic subtypes of Prader–Willi syndrome with growth hormone therapy on intelligence and body mass index

Prader–Willi syndrome (PWS) is a genomic imprinting disorder characterized by infantile hypotonia with a poor suck and failure to thrive, hypogenitalism/hypogonadism, behavior and cognitive problems, hormone deficiencies, hyperphagia, and obesity. The Stanford Binet and Wechsler (WAIS-R; WISC-III) i...

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Publicado en:Am J Med Genet A
Autores principales: Butler, Merlin G., Matthews, Naomi A., Patel, Nidhi, Surampalli, Abhilasha, Gold, June-Anne, Khare, Manaswitha, Thompson, Travis, Cassidy, Suzanne B., Kimonis, Virginia E.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2019
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7737232/
https://ncbi.nlm.nih.gov/pubmed/31313492
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.61293
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