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Related Experiment Videos

Double fingernails on the small fingers.

D Keret, E Ger

    The Journal of Hand Surgery
    |July 1, 1987
    PubMed
    Summary

    This case report details an unusual congenital anomaly: dorsal skin and a fingernail found on the palm side of both small fingers. This rare digital malformation occurred in a child with a normal karyotype, differing from a previously reported similar case linked to a chromosome 6 abnormality.

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    Area of Science:

    • Developmental biology
    • Clinical genetics
    • Congenital anomalies

    Background:

    • Congenital anomalies of the hand and digits are diverse, encompassing variations in structure and formation.
    • Understanding the etiology of rare digital malformations is crucial for genetic counseling and clinical management.
    • Previous literature has documented similar anomalies, sometimes associated with chromosomal abnormalities.

    Observation:

    • This report presents a unique case of bilateral dorsal skin and fingernail presence on the palmar aspect of the small fingers.
    • A normal fingernail was observed on the dorsal surface of the same digits.
    • The affected child exhibited a normal karyotype, indicating the anomaly is not due to major chromosomal aberrations.

    Findings:

    • The primary finding is a rare presentation of ectrodactyly or related digital malformation involving both palmar and dorsal surfaces of the small fingers.
    • The presence of skin and nail tissue in an atypical location (palmar surface) is a key characteristic of this anomaly.
    • The normal karyotype in this case suggests that the etiology may be distinct from previously reported cases linked to chromosomal abnormalities, such as chromosome 6.

    Implications:

    • This case expands the spectrum of known digital anomalies and highlights the variability in their presentation.
    • Further research into the genetic and developmental pathways underlying such anomalies is warranted.
    • Accurate diagnosis and understanding of the underlying mechanisms are essential for providing appropriate clinical care and genetic counseling to affected families.

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