Methylmalonicacidemia with homocystinuria- cbl D
Overview
Methylmalonicacidemia with homocystinuria, cbl D: An inherited organic acid disorder where an enzyme deficiency (cblD) impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of methylmalonic acid and homocystine which results in harmful affects
Symptoms
The list of signs and symptoms mentioned in various sources for Methylmalonicacidemia with homocystinuria, cbl D includes the 14 symptoms listed below: Weakness Reduced blood platelets Numbness in arms Numbness in legs Speech problems Anemia Reduced white blood cells Delirium Behavioral problems Vision problems Kidney problems Confusion Increased blood clotting Tremor Note that Methylmalonicacidemia with homocystinuria, cbl D symptoms usually refers to various symptoms known to a patient, but the phrase Methylmalonicacidemia with homocystinuria, cbl D signs may refer to those signs only noticable by a doctor.