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Trisomy 9 syndrome

Q H Qazi, A Masakawa, C Madahar

    Clinical Genetics
    |October 1, 1977
    PubMed
    Summary
    This summary is machine-generated.

    Mosaic trisomy 9 is a distinct syndrome in infants, characterized by multiple congenital anomalies. Common features include distinctive facial features, microcephaly, and organ system abnormalities, leading to developmental issues.

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    Area of Science:

    • Genetics
    • Pediatrics
    • Developmental Biology

    Background:

    • Mosaic trisomy 9 is a rare chromosomal abnormality.
    • Congenital anomalies are common in infants with chromosomal disorders.
    • Understanding distinct syndromes aids in diagnosis and management.