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Congenital Disorder of Glycosylation Type IIq
A congenital disorder of glycosylation type II that is caused by an autosomal recessive mutation of the COG2 gene on chromosome 1q42.2.
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 congenital disorder of glycosylation type II that is caused by an autosomal recessive mutation of the COG2 gene on chromosome 1q42.2.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.