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Tetraamelia Syndrome 1
A tetraamelia syndrome characterized by complete limb agenesis without defects of scapulae or clavicles that is caused by homozygous or compound heterozygous mutation in WNT3 on chromosome 17q21.31-q21.32.
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Overview
A tetraamelia syndrome characterized by complete limb agenesis without defects of scapulae or clavicles that is caused by homozygous or compound heterozygous mutation in WNT3 on chromosome 17q21.31-q21.32.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.