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Aarskog syndrome.

T Shinkawa, Y Yamauchi, Y Osada

    Urology
    |December 1, 1983
    PubMed
    Summary
    This summary is machine-generated.

    A rare case of Aarskog syndrome, a genetic disorder causing short stature and distinct facial, digital, and genital anomalies, is presented. This highlights the syndrome

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    Area of Science:

    • Genetics
    • Pediatrics
    • Rare Diseases

    Background:

    • Aarskog syndrome is a rare genetic disorder.
    • It is characterized by distinct physical anomalies.

    Observation:

    • This report details a rare case of Aarskog syndrome.
    • The patient presented with characteristic features.

    Findings:

    • The case exemplifies the typical presentation of Aarskog syndrome.
    • Key features include short stature, facial dysmorphia, digital abnormalities, and genital anomalies.

    Implications:

    • This case contributes to the understanding of Aarskog syndrome.
    • It underscores the importance of recognizing characteristic features for diagnosis.