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Related Experiment Videos

The Dubowitz syndrome.

R S Wilroy, R E Tipton, R L Summitt

    American Journal of Medical Genetics
    |January 1, 1978
    PubMed
    Summary
    This summary is machine-generated.

    Dubowitz syndrome is a rare genetic disorder causing growth deficiencies and distinct facial features. This review analyzes reported European cases and personally examined patients to better understand the condition.

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    Area of Science:

    • Clinical Genetics
    • Pediatric Medicine
    • Human Development

    Background:

    • Dubowitz syndrome is an autosomal recessive disorder.
    • Characterized by intrauterine and postnatal growth retardation, microcephaly, and unique facial features.
    • Associated anomalies include developmental delays and genitourinary defects.