Chromosome 1p36 deletion syndrome

A chromosomal anomaly characterized by distinctive facial dysmorphic features, hypotonia, developmental delay, intellectual disability, seizures, heart defects, hearing impairment and prenatal onset growth deficiency.

Also known as: 1p telomere deletion syndrome, 1p36 deletion syndrome, 1p36 microdeletion syndrome, Del(1)(p36), chromosome 1p36 deletion syndrome, distal, isolated cases, deletion 1p36, deletion 1pter, monosomy 1p36

0 clinical trials for this condition and its sub-types, 0 tagged with Chromosome 1p36 deletion syndrome itself.