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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