Please sign in to follow a disease.
Microcephaly 12, primary, autosomal recessive
MONDO:0014484Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CDK6 gene.
Also known as: CDK6 autosomal recessive primary microcephaly, autosomal recessive primary microcephaly caused by mutation in CDK6, microcephaly 12, primary, autosomal recessive, MCPH12
23 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
-
Virtual reality could calm anxious kids with autism at the dentist
Symptom relief ENROLLING_BY_INVITATIONThis study tests whether wearing a virtual reality (VR) headset during dental treatment can reduce fear and stress in children with mild intellectual disabilities or autism spectrum disorder. Two hundred children aged 6 to 12 will either receive standard dental care or use a VR h…
Phase: NA • Sponsor: Semmelweis University • Aim: Symptom relief
Last updated Jun 27, 2026 14:02 UTC
-
Robot suit helps kids with movement disorders take steps at home
Symptom relief OngoingThis study tests a wearable robotic exoskeleton called EXPLORER in 15 children with movement problems from conditions like cerebral palsy. The goal is to see if it helps them walk better in their everyday environments, such as home and the community. The study focuses on safety, …
Phase: NA • Sponsor: MarsiBionics • Aim: Symptom relief
Last updated Jun 27, 2026 07:51 UTC