- cardiac glycogen storage disease
- Pompesches Syndrom n, Pompesche Krankheit f, Glykogenose f Typ III, Kardiomegalia f glykogenica (kardiomegale Form der Glykogenspeicherkrankheit)
Fachwörterbuch Medizin Englisch-Deutsch. 2013.
Fachwörterbuch Medizin Englisch-Deutsch. 2013.
Glycogen storage disease type II — Infobox Disease Name = Glycogen storage disease type II Caption = DiseasesDB = 5296 ICD10 = ICD10|E|74|0|e|70 ICD9 = ICD9|271.0 ICDO = OMIM = 232300 MedlinePlus = eMedicineSubj = med eMedicineTopic = 908 eMedicine mult = eMedicine2|ped|1866 |… … Wikipedia
glycogen storage disease — Pathol. any of several inherited disorders of glycogen metabolism that result in excess accumulation of glycogen in various organs of the body. Also called glycogenosis /gluy koh jeuh noh sis/. * * * or glycogenosis Any of numerous types of… … Universalium
Glycogen 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… … Universalium
Glycogen branching enzyme deficiency — (GBED) is a genetic disease affecting horses, especially American Quarter Horses and related breeds. Diagnosis, Symptoms, and PrognosisLacking an enzyme necessary for storing glycogen, the horse s brain, heart muscle, and skeletal muscles cannot… … Wikipedia
Disease — 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… … Medical dictionary
nervous system disease — Introduction any of the diseases or disorders that affect the functioning of the human nervous system (nervous system, human). Everything that humans sense, consider, and effect and all the unlearned reflexes of the body depend on the… … Universalium
Fabry disease — ICD10 = E75.2 (ILDS E75.25) Classification and external resources Alpha galactosidase the protein that is deficient in Fabry disease … Wikipedia
Danon disease — A genetic disorder characterized by heart problems, mental retardation and muscle weakness that affects males who usually die of cardiac arrhythmia or heart failure at around the age of 30. The disease is due to a deficiency of LAMP 2 (which… … Medical dictionary
endocrine system, human — ▪ anatomy Introduction group of ductless glands (gland) that regulate body processes by secreting chemical substances called hormones (hormone). Hormones act on nearby tissues or are carried in the bloodstream to act on specific target organs… … Universalium
PRKAG2 — Protein kinase, AMP activated, gamma 2 non catalytic subunit, also known as PRKAG2, is a human gene.cite web | title = Entrez Gene: PRKAG2 protein kinase, AMP activated, gamma 2 non catalytic subunit| url =… … Wikipedia
ГЛИКОГЕНОЗЫ — мед. Гликогенозы группа наследственных заболеваний, вызванных недостаточностью одного или нескольких ферментов, вовлечённых в синтез и распад гликогена, и характеризующихся накоплением патологических количеств или типов гликогена в тканях.… … Справочник по болезням