Genetics of Prader-Willi syndrome

Prader–Willi syndrome (PWS) is a complex genomic imprinting disorder associated with a spectrum of medical, cognitive, behavioural, and psychiatric problems and is also the most common cause of life-threatening obesity that can be effectively treated with hormone therapy and restricted diet, if dete...

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Dettagli Bibliografici
Natura:	Online
Lingua:	inglese
Pubblicazione:	MDPI - Multidisciplinary Digital Publishing Institute 2022
Soggetti:	Prader-Willi syndrome appetite treatment Caralluma fimbriata extract single-case Prader–Willi syndrome thromboembolism risk factors vasculitis blood clots registry natural history age diagnosis obesity deletion uniparental disomy genetic syndrome mental illness psychosis major depressive illness obsessive-compulsive disorder autism eating disorder skin picking insurance health claims thrombosis pulmonary embolism deep venous thrombosis individuals with exogenous obesity confirmatory ICD-9 diagnostic codes Prader–Willi 15q11.2 SNORD116 atypical microdeletion food-related behavior childhood scoliosis kyphosis spinal deformities junctional kyphosis treatment options surgery bracing KATP channel activation hyperphagic obesity animal models weight BMI pediatric linear mixed models gut microbiota bacteria fungi diet hyperphagia cross-sectional games parents home exercise bone health Prader-Willi syndrome (PWS) PWS molecular classes PWS genetic subtype–phenotype correlations psychiatric behavioral phenotype growth hormone treatment pharmacogenetic testing cytochrome P450 enzymes drug interactions medication management n/a thema EDItEUR::M Medicine and Nursing
Accesso online:	ONIX_20221117_9783036550268_9
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Genetics of Prader-Willi syndrome

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