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Vitamin B12-responsibe homocystinuria, cblE type (medical condition): An inherited organic acid disorder where an enzyme deficiency (methionine synthase reductase) impairs the body's ability to break down certain proteins consumed in the diet. This results in a buildup of methylmalonic acid and homocystine which results in harmful affects. It is a form of vitamin B12 deficiency.
See also:
Homocystinuria due to defect in methylation cbl e:
»Introduction: Homocystinuria due to defect in methylation cbl e
»Symptoms of Homocystinuria due to defect in methylation cbl e
»Treatments for Homocystinuria due to defect in methylation cbl e
These medical condition or symptom topics may be relevant to medical information for Vitamin B12-responsibe homocystinuria, cblE type:
Vitamin B12-responsibe homocystinuria, cblE type: Another name for Homocystinuria due to defect in methylation cbl e (or close medical condition association).
»Introduction: Homocystinuria due to defect in methylation cbl e
»Symptoms of Homocystinuria due to defect in methylation cbl e
»Treatments for Homocystinuria due to defect in methylation cbl e
Some of the symptoms of Vitamin B12-responsibe homocystinuria, cblE type incude:
Treatments for Vitamin B12-responsibe homocystinuria, cblE type (Homocystinuria due to defect in methylation cbl e) include:
Read more about treatments for Vitamin B12-responsibe homocystinuria, cblE type
Treatment of Vitamin B12-responsibe homocystinuria, cblE type: For more treatment information about Vitamin B12-responsibe homocystinuria, cblE type, see treatment of Homocystinuria due to defect in methylation cbl e (Vitamin B12-responsibe homocystinuria, cblE type)
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