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Up to: Hereditary disease · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Partial deletion of the long arm of chromosome 15
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.
This condition has no sub-types.