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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, 0 tagged with Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 itself.

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↑ Prader-Willi syndrome due to paternal 15q11q13 deletion (0)

Including sub-types (1) Tagged with Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2 (0)

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…

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

Last updated Jun 27, 2026 12:05 UTC