Monosomy 5p

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.

Cat cry

The presence of a characteristic high-pitched cry that sounds similar to the meowing of a kitten.


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(per page)
PMID (PMCID)
15844774
 FEMALE Child
A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.
Posmyk R, Panasiuk B, Yatsenko SA, Stankiewicz P, Midro AT.
Genet Couns. 2005;16(1):17-25.
A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.
15844774
 FEMALE Child
A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.
Posmyk R, Panasiuk B, Yatsenko SA, Stankiewicz P, Midro AT.
Genet Couns. 2005;16(1):17-25.
A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-up.
2677233
 MALE Infant, Newborn
[The cat cry (cri du chat) syndrome: report of a case with review of 10 cases at the National Taiwan University Hospital].
Chuang SM, Wang TR, Jean HH, Lee FY.
Taiwan Yi Xue Hui Za Zhi. 1989;88(6):635-8, 628-9.
[The cat cry (cri du chat) syndrome: report of a case with review of 10 cases at the National Taiwan University Hospital].
2677233
 MALE Infant, Newborn
[The cat cry (cri du chat) syndrome: report of a case with review of 10 cases at the National Taiwan University Hospital].
Chuang SM, Wang TR, Jean HH, Lee FY.
Taiwan Yi Xue Hui Za Zhi. 1989;88(6):635-8, 628-9.
The cat cry (cri du chat) syndrome is a rare congenital anomaly due to partial deletion of the short arm of the No.