Glycogen storage disease type III
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Glycogen storage disease type III
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Introduction to the skeletal system
Introduction to the cardiovascular system
Introduction to the muscular system
Anatomical terminology
Anatomy of the muscles and nerves of the posterior abdominal wall
Anatomy of the abdominal viscera: Innervation of the abdominal viscera
Enteric nervous system
Physiological changes during exercise
Pentose phosphate pathway
Glycolysis
Electron transport chain and oxidative phosphorylation
Development of the face and palate
Pharyngeal arches, pouches, and clefts
Development of the teeth
Development of the tongue
Citric acid cycle
Gluconeogenesis
Nitrogen and urea cycle
Amino acid metabolism
Fatty acid synthesis
Ketone body metabolism
Fatty acid oxidation
Cholesterol metabolism
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Gaucher disease (NORD)
Cystinosis
Ornithine transcarbamylase deficiency
Familial hypercholesterolemia
Disorders of carbohydrate metabolism: Pathology review
Dyslipidemias: Pathology review
Glycogen storage disorders: Pathology review
Disorders of fatty acid metabolism: Pathology review
Lysosomal storage disorders: Pathology review
Disorders of amino acid metabolism: Pathology review
Carbohydrates and sugars
Proteins
Fats and lipids
Vitamin B12 deficiency
Fat-soluble vitamin deficiency and toxicity: Pathology review
Water-soluble vitamin deficiency and toxicity: B1-B7: Pathology review
Zinc deficiency and protein-energy malnutrition: Pathology review
Nernst equation
Nernst equation
Peroxisomal disorders: Pathology review
Peroxisomal disorders: Pathology review
Nuclear structure
Nuclear structure
Amino acids and protein folding
Amino acids and protein folding
Nucleotide metabolism
Nucleotide metabolism
Mitosis and meiosis
Mitosis and meiosis
Adenosine deaminase deficiency
Adenosine deaminase deficiency
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
ELISA (Enzyme-linked immunosorbent assay)
DNA cloning
Fluorescence in situ hybridization
Gel electrophoresis and genetic testing
Lactose intolerance
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Huntington disease
Fragile X syndrome
Myotonic dystrophy
Friedreich ataxia
Prader-Willi syndrome
Angelman syndrome
Polycystic kidney disease
Familial adenomatous polyposis
Alpha-thalassemia
Beta-thalassemia
Miscellaneous genetic disorders: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Autosomal trisomies: Pathology review
Mitochondrial myopathy
Gestational diabetes
Placental abruption
Preeclampsia & eclampsia
Fetal alcohol syndrome
Testicular tumors: Pathology review
Disorders of sex chromosomes: Pathology review
Prostate disorders and cancer: Pathology review
Uterine disorders: Pathology review
Cervical cancer: Pathology review
Ovarian cysts and tumors: Pathology review
Vaginal and vulvar disorders: Pathology review
Breast cancer: Pathology review
Congenital TORCH infections: Pathology review
Disorders of sexual development and sex hormones: Pathology review
Complications during pregnancy: Pathology review
Amenorrhea: Pathology review
Adrenergic antagonists: Alpha blockers
Androgens and antiandrogens
PDE5 inhibitors
Aromatase inhibitors
Uterine stimulants and relaxants
Estrogens and antiestrogens
Progestins and antiprogestins
Key Takeaways
Glycogen storage disease type III is one of the genetic disorders affecting how the body stores and uses glycogen. People with glycogen storage disease type III have a deficiency of the glycogen debrancher enzyme (α-1,6-glucosidase), one of the enzymes that help to break down glycogen. The symptoms of glycogen storage disease type III generally appear during childhood and include generalized muscle weakness, hepatosplenomegaly, fasting hypoglycemia, and ketosis.