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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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| Опубликовано в: : | Am J Med Genet A |
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| Главные авторы: | , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2019
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| Предметы: | |
| Online-ссылка: | 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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