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Related Experiment Videos

Familial 5p- syndrome.

T Kushnick, K W Rao, A N Lamb

    Clinical Genetics
    |November 1, 1984
    PubMed
    Summary
    This summary is machine-generated.

    A mother and son with a terminal deletion on chromosome 5 (del(5)(qter----p15.1)) showed mild features. Unlike classical Cri-du-Chat Syndrome, they lacked severe intellectual and growth deficits.

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    Area of Science:

    • Genetics
    • Human Chromosome Abnormalities
    • Clinical Dysmorphology

    Background:

    • Cri-du-Chat Syndrome is a genetic disorder caused by a deletion on the short arm of chromosome 5.
    • Classical Cri-du-Chat Syndrome is characterized by severe intellectual disability, growth retardation, and distinctive facial features.