CDGIn (medical condition): A very rare inherited metabolic disorder where defective carbohydrate compounds are attached to glycoproteins and thus impairing glycoprotein function. Type 1n involves a defect in the RFT1 gene and is characterized mainly by enlarged liver, seizures, developmental delay, reduced muscle tone and abnormal blood coagulation.
See also:
Congenital disorder of glycosylation, type In:
»Introduction: Congenital disorder of glycosylation, type In
»Symptoms of Congenital disorder of glycosylation, type In
CDGIn: Another name for Congenital disorder of glycosylation, type In (or close medical condition association).
»Introduction: Congenital disorder of glycosylation, type In
»Symptoms of Congenital disorder of glycosylation, type In
Some of the symptoms of CDGIn incude:
Read more about symptoms of CDGIn (Congenital disorder of glycosylation, type In)
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