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MYH10-related neurodevelopmental disorder with congenital anomalies

MONDO:0700281

An autosomal dominant complex neurodevelopmental disorder in which the cause of the disease is a mutation in the MYH10 gene.

1 clinical trial for this condition and its sub-types, 0 tagged with MYH10-related neurodevelopmental disorder with congenital anomalies itself.

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↑ Autosomal dominant disease (699) ↑ Mendelian neurodevelopmental disorder (208) ↑ Complex neurodevelopmental disorder with or without congenital anomalies (0)

Including sub-types (1) Tagged with MYH10-related neurodevelopmental disorder with congenital anomalies (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