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Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2

MONDO:0015784

Also known as: Prader-Willi Syndrome (Type 2)

1 clinical trial for this condition and its sub-types.

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Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Neurodevelopmental disorder (147) Endocrine system disorder (72) Hypogonadism (45) Prader-Willi syndrome (30) Syndromic disease (25) Hereditary endocrine growth disease (24) Hypogonadotropic hypogonadism (18)

New parent support programme shows promise for families of children with complex needs

Symptom relief Completed

This pilot study tested a community-based group programme called 'Encompass' for parents of children under 5 with complex neurodisability. Fifteen parents in East London attended ten group sessions over six months. The study aimed to see if the programme was feasible and acceptab…

Phase: NA • Sponsor: City, University of London • Aim: Symptom relief

Last updated Jun 27, 2026 12:05 UTC