Monosomy 5p syndrome
ORPHA:281· ICD-10 Q93.4
Definition
A rare developmental defect during embryogenesis, resulting from partial or total deletion of the short arm of chromosome 5, classically characterized by a high-pitched, monotone, cat-like cry (cri du chat) present since birth, associated with varying degrees of intellectual disability, developmental delay, microcephaly, and facial dysmorphism.
- Prevalence
- Unknown
- Inheritance
- Not applicable, Unknown
- Age of onset
- Antenatal