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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...

Description complète

Enregistré dans:
Format: Online
Langue:anglais
Publié: MDPI - Multidisciplinary Digital Publishing Institute 2022
Sujets:
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
Accès en ligne:ONIX_20221117_9783036550268_9
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