Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Chromosome 1q deletion · Holoprosencephaly
Chromosome 1q41-q42 deletion syndrome
1q41q42 microdeletion syndrome is a chromosomal anomaly characterized by a severe developmental delay and/or intellectual disability, typical facial dysmorphic features, brain anomalies, seizures, cleft palate, clubfeet, nail hypoplasia and congenital heart disease.
This condition has no sub-types.