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Chromosome 15q24 deletion syndrome
rare15q24 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.
- Identifiers
- MONDO:0013256 OMIM:613406Orphanet:94065
- Causal genes
- SIN3A
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the long arm of chromosome 15
- Also known as
- 15q24 microdeletion syndrome · 15q24 recurrent microdeletion syndrome · Del(15)(q24) · monosomy 15q24 · WITKOS
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