15q24 microdeletion syndrome (Orphanet_94065) 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: Del(15)(q24), Monosomy 15q24.