brancher glycogen storage disease
1Glycogen storage disorders — ▪ Table Glycogen storage disorders (GSDs) type enzyme defect clinical features type I (von Gierke disease) glucose 6 phosphatase hypoglycemia, enlarged liver and kidneys, gastrointestinal symptoms, nosebleeds, short stature, gout type II (Pompe… …
2brancher deficiency — glycogen storage disease, type IV …
3brancher deficiency glycogenosis — glycogen storage disease, type IV …
4Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… …
5brancher enzyme deficiency — branch·er en·zyme de·fi·cien·cy (branchґər enґzīm) glycogen storage disease, type IV …
6glycogenosis — Any of the glycogen deposition diseases characterized by accumulation of glycogen of normal or abnormal chemical structure in tissue; there may be enlargement of the liver, heart, or striated muscle, including the …
7deficiency — An insufficient quantity of some substance (as in dietary d. or hemoglobin d. in marrow aplasia); organization (as in mental d.); activity (as in enzyme d. or reduced oxygen carrying capacity of the blood), etc., of which the amount present is of …
814-α-glucan branching enzyme — 1,4 α glu·can branch·ing en·zyme (glooґkan branchґing enґzīm) [EC 2.4.1.18] an enzyme of the transferase class that catalyzes the cleavage of internal α 1,4 glucoside linkages in glycogen (or, in plants, amylopectin) and transfer… …
