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Name Prader-Willi Syndrome
Related to/Also known as HHHO Syndrome
Symptoms of Prader-Willi syndrome
 Prader-Willi syndrome is a genetic disorder, which is present from birth. It is characterised by a number of behavioural and psychological features, including low muscle tone, excessive appetite (leading to obesity if not controlled), and immature physical development . Most have borderline or moderate learning difficulties.
Types  
Useful national contacts PWSA-UK (Prader-Willi Syndrome Association)
Link opens in new window www.pwsa.co.uk
Tel: 01332 365676
Children & young people PWS by age (PWSA-UK)
Link opens in new windowwww.pwsa.co.uk/pws-by-agecfc0767f
Online resources

Link opens in new window Easy-Read guide to Coronavirus from Mencap

Prader-Willi syndrome (NHS Choices)
Link opens in new window https://tinyurl.com/c7wl5z6
Living with a condition (The Brain Charity)
News and Events  
Our resources The library at The Brain Charity has a range of resources on Prader-Willi syndrome and on a wide range of disability-related issues.
Learning disorders Muscles Genetic disorders Rare conditions