Genetics of Prader-Willi syndrome

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