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Up to: Syndromic disease · Partial deletion of the short arm of chromosome 5
Cri-du-chat syndrome
Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism.
This condition has no sub-types.