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Meier-Gorlin Syndrome 9
A Meier-Gorlin syndrome that is characterized by short stature, microtia, and patellar hypoplasia or absence and that is caused by homozygous or compound heterozygous mutation in the GINS3 gene on chromosome 16q21.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
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Overview
A Meier-Gorlin syndrome that is characterized by short stature, microtia, and patellar hypoplasia or absence and that is caused by homozygous or compound heterozygous mutation in the GINS3 gene on chromosome 16q21.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.