Aarskog syndrome

Changed by Daniel J Bell, 26 Oct 2018

Updates to Article Attributes

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Aarskog syndrome or Aarskog–Scott syndrome (also known as the facio-digito-genital syndrome) is a rare anomaly characterized by short stature in association with a variety of structural anomalies involving mainly the face, distal extremities, and external genitalia.

Epidemiology

Population prevalence is estimated to be 1/25,000

Clinical presentation

The major manifestations of this syndrome include

Pathology

Genetics

It commonly carries an X-linked inheritance. However, sex-influenced autosomal dominant inheritance is also possibleseen in some families. The FDG1 gene on the X chromosome-chromosome is the only known gene associated with Aarskog syndrome (22% of affected males). 

  • -</ul><h4>Pathology</h4><h5>Genetics</h5><p>It commonly carries an X-linked inheritance. However, sex-influenced autosomal dominant inheritance is also possible in some families. The FDG1 gene on the X chromosome is the only known gene associated with Aarskog syndrome (22% of affected males). </p><h4> </h4>
  • +</ul><h4>Pathology</h4><h5>Genetics</h5><p>It commonly carries an X-linked inheritance. However, sex-influenced autosomal dominant inheritance is also seen in some families. The <em>FDG1</em> gene on the X-chromosome is the only known gene associated with Aarskog syndrome (22% of affected males). </p><h4> </h4>

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