Chromosome 15q24 deletion syndrome

15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.

Also known as: 15q24 microdeletion syndrome, 15q24 recurrent microdeletion syndrome, Del(15)(q24), chromosome 15q24 deletion syndrome, monosomy 15q24, WITKOS, Witteveen-Kolk syndrome, chromosome 15Q24 Duplication syndrome

1 clinical trial for this condition and its sub-types, 1 tagged with Chromosome 15q24 deletion syndrome itself.