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2,012 Possible Causes for Glycogen Storage Disease Type 2

  • Glycogen Storage Disease due to Glucose-6-Phosphat Transport Defect

    The following points highlight the top ten types of glycogen storage diseases. The types are: 1. von Gierke’s Disease 2. Pompe’s Disease 3. Amylopectinosis 4.[biologydiscussion.com] Gastroenterology. 1991 Feb;100(2):549-54. PMID: 1985051 Chronic inflammatory bowel disease in glycogen storage disease type 1B.[humpath.com] Current methods of unequivocally diagnosing type 1b and type 1c glycogen storage disease are indirect and complex. 3.[clinsci.org]

  • Glycogen Storage Disease Type 2

    Glycogen storage disease type 2, also known as Pompe disease or acid maltase deficiency disease, is an inherited metabolic disorder. [1] [2] [3] While glycogen storage disease[rarediseases.info.nih.gov] Glycogen storage disease type 2, sometimes also referred to as Pompe disease, is a genetic disorder inherited as an autosomal recessive trait.[symptoma.com] Title: Late-Onset Glycogen Storage Disease Type 2 VOLUME: 14 ISSUE: 8 Author(s): M. Filosto, M.S. Cotelli, V. Vielmi, A. Todeschini, F. Rinaldi, S. Rota, M.[eurekaselect.com]

  • Glycogen Storage Disease

    […] deficiency Glycogen storage disease Glycogen storage disease type III Glycogen storage disease type VIII Glycogen storage disease, type 1 Glycogen storage disease, type 2[icd9data.com] […] of Glycogen Storage Disease Type 1a for at risk couples.[questdiagnostics.com] type 0-muscle 611556 AR GYS2 Glycogen synthase 2 (glycogen storage disease 0, liver) 240600 AR LAMP2 Glycogen storage disease type IIb-Danon disease 300257 XLD LDHA Glycogen[mayomedicallaboratories.com]

  • Glycogen Storage Disease Type 1

    […] of Glycogen Storage Disease Type 1a for at risk couples.[questdiagnostics.com] […] deficiency Glycogen storage disease Glycogen storage disease type III Glycogen storage disease type VIII Glycogen storage disease, type 1 Glycogen storage disease, type 2[icd9data.com] Treating Glycogen storage disease type I Risk calculators and risk factors for Glycogen storage disease type I Editor-In-Chief: C.[wikidoc.org]

  • Glycogen Storage Disease Type 4

    […] deficiency Glycogen storage disease Glycogen storage disease type III Glycogen storage disease type VIII Glycogen storage disease, type 1 Glycogen storage disease, type 2[icd9data.com] Glycogen storage diseases in general are very few, around 2 per 1,00,000 children. Glycogen storage disease type 4 is rarer.[symptoma.com] Disease Type VI (Hers Disease) Liver Phosphorylase deficiency Findings: 1) Hepatomegaly 2) Mild fasting hypoglycemia Not bad Glycogen Storage Disease Type VII (Tarui Disease[quizlet.com]

  • Glycogen Storage Disease Type 5

    The following points highlight the top ten types of glycogen storage diseases. The types are: 1. von Gierke’s Disease 2. Pompe’s Disease 3. Amylopectinosis 4.[biologydiscussion.com] […] deficiency Glycogen storage disease Glycogen storage disease type III Glycogen storage disease type VIII Glycogen storage disease, type 1 Glycogen storage disease, type 2[icd9data.com] (disorder) Glycogen storage disease, type IV Glycogen storage disease, type IX Glycogen storage disease, type V Glycogen storage disease, type VI Glycogen storage disease,[icd9data.com]

  • Glycogen Storage Disease Type 7

    […] deficiency Glycogen storage disease Glycogen storage disease type III Glycogen storage disease type VIII Glycogen storage disease, type 1 Glycogen storage disease, type 2[icd9data.com] Additional molecular genetic analyses confirmed glycogen storage disease Type IV with the finding of compound heterozygosity for 2 mutations (c.691 2T C and c.1570C T, p.R524X[journals.lww.com] (von Gierke disease) glycogen storage disease type 1b (GSD1b) (MIM.232220) glycogen storage disease type 1c (GSD1c) (MIM.232240) glycogen storage disease type 2 (GSD2) (MIM[humpath.com]

  • Glycogen Storage Disease Type 3

    The following points highlight the top ten types of glycogen storage diseases. The types are: 1. von Gierke’s Disease 2. Pompe’s Disease 3. Amylopectinosis 4.[biologydiscussion.com] storage disease type III.[cmaj.ca] "Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome".[en.wikipedia.org]

  • Glycogen Storage Disease Type 6

    […] deficiency Glycogen storage disease Glycogen storage disease type III Glycogen storage disease type VIII Glycogen storage disease, type 1 Glycogen storage disease, type 2[icd9data.com] The following points highlight the top ten types of glycogen storage diseases. The types are: 1. von Gierke’s Disease 2. Pompe’s Disease 3. Amylopectinosis 4.[biologydiscussion.com] Mol Genet Metab. 2003 Jun. 79(2):142-5. [Medline]. Jagadisan B, Ranganath P. Glycogen Storage Disease Type VI With a Novel Mutation in PYGL Gene.[emedicine.com]

  • Glycogen Storage Disease Type 0

    Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia[ncbi.nlm.nih.gov] disease type 0 is most commonly diagnosed during infancy and early childhood. [2] References [ edit ] External links [ edit ] Media related to Glycogen storage disease type[en.wikipedia.org] 4 A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0. ( 20051115 ) Soggia A.P....Pereira M.A. 2010 5 The variable clinical phenotype[malacards.org]

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