The Cri du Chat syndrome (CdCS) is a genetic disease resulting from a deletion of variable size occurring on the short arm of chromosome 5 (5p-). The incidence ranges from 1:15,000 to 1:50,000
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Cri-du-chat syndrome (CdCS; OMIM #123450) is a rare genetic syndrome caused by partial or total deletion of the short arm of chromosome 5 (5p-) with an incidence ranging from 1:15,000 to 1:50,000 live births. had psychotic symptoms at the age of 62 years. Disability status examination indicated that she had moderate intellectual
Keywords: 5p deletion, Cri‐du‐chat syndrome, prenatal diagnosis, single nucleotide polymorphism array. This study provides clinical and molecular characterization for 12 prenatal case of Cri‐du‐chat syndrome (CdCS) and genotyping‐phenotyping analysis for these cases. The findings from the present study are important for genetic
Cat cry at birth, small head, wide eyes signal disabling "cri du chat" syndrome. By ABC News. October 12, 2008, 12:23 PM. Oct. 13, 2008 -- In 1988, Katie Castillo was born with the cord around her
Cri du chat Feedback: The clinical symptoms of cri du chat syndrome usually include a high-pitched cat-like cry, mental retardation, delayed development, distinctive facial features, small head size (microcephaly), widely-spaced eyes (hypertelorism), low birth weight and weak muscle tone (hypotonia) in infancy.
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symptoms of cri du chat
