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Congenital Disorder of Glycosylation Type IIm
A congenital disorder of glycosylation type II that is characterized by infantile onset seizures, hypsarrhythmia, hypotonia, and severe intellectual disability with lack of speech and that is caused by X-linked dominant
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Overview
A congenital disorder of glycosylation type II that is characterized by infantile onset seizures, hypsarrhythmia, hypotonia, and severe intellectual disability with lack of speech and that is caused by X-linked dominant
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.