Last Updated: 8 August 2024
Acromicric Dysplasia
Last Updated: 8 August 2024
Acromicric Dysplasia
Acromicric dysplasia is a rare genetic disorder characterised by short stature, short hands and feet, and distinctive facial features. It is caused by mutations in the FBN1 gene. Other symptoms may include joint stiffness and skin anomalies. Diagnosis is typically confirmed through genetic testing. Treatment focuses on managing symptoms.
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Acromicric Dysplasia
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