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New chromosomal dysmorphic syndromes. 2. Trisomy 10p

S Stengel-Rutkowski, J D Murken, R Frankenberger

    European Journal of Pediatrics
    |October 12, 1977
    PubMed
    Summary

    A mother's balanced translocation t(5;10)(p15;p13) resulted in two children with trisomy 10p, a condition characterized by a distinct dysmorphic syndrome. This genetic finding confirms a recognizable pattern of anomalies associated with trisomy 10p.

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    Area of Science:

    • Genetics
    • Clinical Dysmorphology
    • Human Reproduction

    Background:

    • Balanced translocations can lead to unbalanced chromosomal constitutions in offspring.
    • Parental chromosomal abnormalities are a significant cause of recurrent miscarriages and congenital anomalies.
    • Trisomy 10p is a rare chromosomal disorder with variable clinical manifestations.