3p25.3 microdeletion syndrome

MONDO:0018564

A rare chromosomal anomaly characterized by intellectual disability, epilepsy or EEG abnormalities, poor speech, ataxia, and stereotypic hand movements.

Also known as: Del(3)p(25.3), intellectual disability-epilepsy-stereotypic hand movement syndrome, monosomy 3p25.3

0 clinical trials for this condition and its sub-types, 0 tagged with 3p25.3 microdeletion syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Partial deletion of the short arm of chromosome 3 (0)

Including sub-types (0) Tagged with 3p25.3 microdeletion syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.