Glycogen Storage Disease Type 7 Causes & Reasons

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Glycogen Storage Disease Type 7 Symptom Checker: Possible causes include Glycogen Storage Disease due to Glucose-6-Phosphat Transport Defect. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search.

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Possible Causes

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

Glycogen Storage Diseases: Type # 7. Lactosuria : Lactosuria occurs in women during the period of lactation. [biologydiscussion.com]

Neutropenia and impaired neutrophil migration in type IB glycogen storage disease. J Pediatr 1980 ;97: 906 –10. 6. [nejm.org]

Current methods of unequivocally diagnosing type 1b and type 1c glycogen storage disease are indirect and complex. 3. [clinsci.org]

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Glycogen Storage Disease Type 7

There are no guidelines for the prevention of Glycogen storage disease type 7. [symptoma.com]

Glycogen storage disease type 7 (GSD7) is an inherited condition in which the body is unable to break down glycogen (a complex sugar) in the muscle cells. [rarediseases.info.nih.gov]

Prognosis - Glycogen storage disease type 7 Prognosis of Glycogen storage disease type 7: good with treatment.The \'prognosis\' of Glycogen storage disease type 7 usually [checkorphan.org]

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Glycogen Storage Disease

H Histopathology of glycogen storage disease ‎ (15 F) T Glycogen storage disease type 0 ‎ (1 F) Glycogen storage disease type I ‎ (6 F) Glycogen storage disease type II ‎ [commons.wikimedia.org]

Glycogen storage disease, type 3 Glycogen storage disease, type 4 Glycogen storage disease, type 5 Glycogen storage disease, type 6 Glycogen storage disease, type 7 Glycogen [icd9data.com]

This 7-year-old Japanese girl, diagnosed with glycogen storage disease Type 1a at the age of 2 years, presented with repeated transient ischemic attacks. [ncbi.nlm.nih.gov]

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Glycogen Storage Disease Type 1

storage disease type viii Glycogen storage disease, type 4 Glycogen storage disease, type 6 Glycogen storage disease, type 7 Glycogen storage disease, type 8 Glycogen storage [icd10data.com]

Mutations in the glucose-6-phosphatase-alpha (G6PC) gene that cause type Ia glycogen storage disease. Chou JY, Mansfield BC. Hum Mutat. 2008 Jul;29(7):921-30. [atlasgeneticsoncology.org]

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Glycogen Storage Disease Type 4

Glycogen storage disease type IV: a case report. Chung Hua I Hsueh Tsa Chih (Taipei). 1999 Oct. 62(10):743-7. [Medline]. Chen Y. Glycogen Storage Diseases. [emedicine.medscape.com]

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Glycogen Storage Disease Type 2

Pompe Controllo di autorità Q1365789 Reasonator Scholia Statistica File nella categoria "Glycogen storage disease type II" Questa categoria contiene 7 file, indicati di seguito [commons.wikimedia.org]

[…] 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]

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Glycogen Storage Disease Type 5

Glycogen Storage Diseases: Type # 7. Lactosuria : Lactosuria occurs in women during the period of lactation. [biologydiscussion.com]

Glycogen Storage Diseases: Type # 1. von Gierke’s Disease : a. [biologydiscussion.com]

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Glycogen Storage Disease Type 6

Glycogen Storage Disease Type VI. 2009 Apr 23 [updated 2011 May 17]. [ghr.nlm.nih.gov]

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Glycogen Storage Disease Type 3

Glycogen Storage Diseases: Type # 7. Lactosuria : Lactosuria occurs in women during the period of lactation. [biologydiscussion.com]

Glycogen storage disease type III diagnosis and management guidelines. Genet Med. 2010 Jul;12(7):446-63. doi: 10.1097/GIM.0b013e3181e655b6. Lucchiari, S., et al. [rarediseases.org]

BACKGROUND: Type 3 glycogen storage disease is an inborn error of metabolism in young infants that often requires extensive workup. [ncbi.nlm.nih.gov]

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Glycogen Storage Disease Type 0

Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations. [emedicine.com]

Types [ edit ] There are two types of this\\e condition glycogen storage disease type 0 to be considered, they are: [3] [4] Glycogen storage disease due to liver glycogen [en.wikipedia.org]

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Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency

Get Update Overview Glycogen storage disease VII is an autosomal recessive metabolic disorder characterized clinically by exercise intolerance, muscle cramping, exertional [diseaseinfosearch.org]

External links Glycogen storage disease type 7; Muscle phosphofructokinase deficiency; Tarui disease at NIH 's Office of Rare Diseases Asociación Española de Enfermos de Glucogenosis [infogalactic.com]

6 Glycogen storage disease type 7 Glycogen storage disease type 9 Glycogen storage disease type 9A Glycogen storage disease type 9B Glycogen storage disease type 9C Glycogen [orpha.net]

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Glycogen Storage Disease due to GLUT2 Deficiency

Glycogen storage disease type 7[?] Glycogen storage disease type 9[?] Glycogen storage disease type II[?] Glycogen storage disease type V[?] [encyclopedia.kids.net.au]

Storage Disease Type 7 PFK-1 Deficiency (Tarui's Disease) Generation of ATP in glycolysis from glucose or G1P is inhibited Muscle cramping and exercise intolerance ( more [studyblue.com]

storage disease, glucose transporter2 (glut2) Abstract: Fanconi-Bickel syndrome (FBS, OMIM 227810) is a rare type of glycogen storage disease (GSD). [doi.org]

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Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

Let’s try to break the topic, simplify it and cover all the important aspects of Glycogen Storage Diseases (GSD). 7 types of Glycogen Storage Diseases Mnemonic: VP CAM HT. [epomedicine.com]

Bone mineralisation in type 1 glycogen storage disease. Eur J Pediatr 1995;154:483-7. [ PubMed ] Jun HS, Weinstein DA, Lee YM, et al. [tp.amegroups.com]

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Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

Glycogen storage disease type 5 PYGM Glycogen storage disease type 6B PYGL Glycogen storage disease type 7 PFKM Glycogen storage disease type 9A PHKA2 Glycogen storage disease [centogene.com]

Phosphoglycerate mutase (PGAM) deficiency (glycogen storage disease type X) has been reported in 12 patients of whom 9 were African American. [ncbi.nlm.nih.gov]

[…] rdfs:seeAlso sameAs GLYCOGEN STORAGE DISEASE, TYPE IXd; GSD9D [omim:300559] dcterms:title GLYCOGEN STORAGE DISEASE, TYPE IXd; GSD9D dcterms:description Glycogen storage disease [bio2rdf.org]

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Glycogen Storage Disease due to Phosphoglycerate Kinase 1 Deficiency

Storage Disease Type V / diagnosis* Glycogen Storage Disease Type VII / diagnosis* Humans Male Metabolism, Inborn Errors / diagnosis*, enzymology*, urine Muscle, Skeletal [biomedsearch.com]

"Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VI". Hum Mol Genet. 7 (5): 865–70. PMID 9536091. Dagli AI, Weinstein DA. [wikidoc.org]

[…] in glycogen storage disease type VI. [link.springer.com]

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Adult Polyglucosan Body Disease

Glycogen storage disease type IV, is a form of glycogen storage disease, which is caused by an inborn error of metabolism. [en.wikipedia.org]

Epidemiology Frequency International Glycogen-storage disease type IV represents an uncommon form of glycogen-storage disease. [emedicine.medscape.com]

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Glycogen Storage Disease Type 9

Disorders of gluconeogenesis include: fructose-1,6-bisphosphatase deficiency, pyruvate dehydrogenase complex deficiency, and glycogen storage disease type I. 7. [ncbi.nlm.nih.gov]

disease References [ edit ] a b "Glycogen storage disease type IX". [en.wikipedia.org]

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Polyglucosan Body Myopathy Type 2

Chapter First Online: 06 October 2017 Abstract Defects in enzymes involved in glycogen metabolism result in glycogen storage diseases (GSDs), which may affect the skeletal [link.springer.com]

storage disease Gyg1, Gys2 Glycogen Storage Disease 0, Liver Gys2 Glycogen Storage Disease 0, Muscle Gys1 glycogen storage disease IV Gbe1 Glycogen Storage Disease XIV Pgm1 [rgd.mcw.edu]

A new muscle glycogen storage disease associated with glycogenin-1 deficiency. Ann Neurol. 2014;76:891–8. CrossRef PubMed PubMedCentral Google Scholar 3. [link.springer.com]

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Danon Disease

2 deficiency Glycogen storage disease type 2b (formerly) Lysosomal Glycogen Storage Disease Without Acid Maltase Deficiency Lysosomal glycogen storage disease with normal [wikidata.org]

A patient with lysosomal glycogen storage disease with normal acid maltase (translation). [doi.org]

Storage Disease Type IIb/genetics* Glycogen Storage Disease Type IIb/metabolism High-Throughput Nucleotide Sequencing Humans Infant Lysosomal-Associated Membrane Protein [ncbi.nlm.nih.gov]

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Hepatocellular Adenoma

Abstract The development of hepatocellular adenoma has been recognized in association with glycogen storage disease type I and, less often, with glycogen storage disease type [ncbi.nlm.nih.gov]

AIMS: Glycogen storage disease type I is a metabolic disorder resulting from deficiency of the glucose-6-phosphate complex. [ncbi.nlm.nih.gov]

Hepatic adenoma in type Ia glycogen storage disease. Arch Pathol Lab Med 1987;111:166–169PMID : 3545138. 7. Leese T, Farges O, Bismuth H. [kjim.org]

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Disorder of Carbohydrate Metabolism

Al-Azzeh PhD in Human Nutrition Food Science Umm Al-Qura University Department of Clinical Nutrition 26 Glycogen Storage Diseases Glycogen Storage Diseases (GSD) Deficiencies [powershow.com]

Jiffri 2 Glycogen Storage Diseases (Glycogenoses) -Glycogen storage diseases are a group of inherited conditions characterized by tissue deposits of glycogen that are abnormal [slideplayer.com]

[…] term(s): Type V glycogen storage disease E74.09 Other glycogen storage disease Inclusion term(s): Andersen disease Hers disease Tauri disease Glycogen storage disease, types [icd10coded.com]

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Muscular Dystrophy-Dystroglycanopathy Type C7

Storage Disease Hemiplegic Migraine Joubert Syndrome L1 Syndrome Lethal Multiple Pterygium Syndrome Leukoencephalopathy Limb-Girdle Muscular Dystrophy Malignant Hyperthermia [preventiongenetics.com]

Bilateral perisylvian polymicrogyria Oguchi disease Fish-eye disease Weissenbacher-Zweymuller syndrome Glycogen storage disease type 7 GM1 gangliosidosis type 2 Jones syndrome [checkrare.com]

storage disease II - GSDII Limb-Girdle, Muscular dystrophy, type 2W - (AR) 1.43 LIM and senescent cell antigen-like domains 2 * Limb-Girdle, Muscular dystrophy, type 2W - [195.83.227.65]

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Disorder of Fructose Metabolism

Glycogen Storage Diseases: Type # 7. Lactosuria : Lactosuria occurs in women during the period of lactation. [biologydiscussion.com]

storage disease E74.01 von Gierke disease E74.09 Other glycogen storage disease E74.1 Disorders of fructose metabolism E74.10 Disorder of fructose metabolism, unspecified [icd10data.com]

Keywords Lactic Acidosis Infant Formula Glycogen Storage Disease Fructose Ingestion Invert Sugar These keywords were added by machine and not by the authors. [link.springer.com]

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Hypoglycemia

disease type 1b); debrancher deficiency (glycogen-storage disease type III); hepatic phosphorylase deficiency (glycogen-storage disease type VI); glycogen synthase deficiency [emedicine.com]

Disorders of hepatic glucose production include glucose-6-phosphatase deficiency (glycogen-storage disease type Ia); glucose 6-phosphate translocase deficiency (glycogen storage [emedicine.com]

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Hereditary Myopathy with Lactic Acidosis due to ISCU Deficiency

storage disease GAA Glycogen storage disease GBE1 Glycogen storage disease GYG1 Glycogen storage disease GYS1 Glycogen storage disease GYS2 Glycogen storage disease LAMP2 [genda.com.ar]

Storage Disease 0, Muscle (GSD0B) Glycogen Storage Disease IIIa; Glycogen Storage Disease IIIb Glycogen Storage Disease IV Glycogen Storage Disease IXc (GSD9C) Glycogen Storage [nextgenerationsequencing.info]

storage disease AR 193 573 GBE1 Glycogen storage disease AR 36 70 GYG1 Glycogen storage disease, Polyglucosan body myopathy 2 AR 9 16 GYS1 Glycogen storage disease AR 8 5 [blueprintgenetics.com]

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Disorders of Pyruvate Metabolism and Gluconeogenesis

Abstract Abstract Glycogen storage diseases are inherited disorders that affect glycogen metabolism. [ommbid.mhmedical.com]

Mutations in this gene cause glycogen storage disease type I (GSD1). [genecards.org]

H01953 ] Glycogen storage disease type XIV [DS: H01954 ] Glycogen storage disease type XV [DS: H01955 ] Glycogen storage disease type 0a [DS: H01950 ] Glycogen storage disease [genome.jp]

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Proximal Renal Tubular Acidosis

Sidbury, Renal Disease in Type I Glycogen Storage Disease, New England Journal of Medicine, 318, 1, (7), (1988). [doi.org]

Abstract A 2 1/2-year-old Japanese boy with glycogen storage disease, type 9, developed proximal renal tubular acidosis (RTA). [ncbi.nlm.nih.gov]

Causes Familial disorders Cystinosis [2] Galactosemia [3] Glycogen storage disease (type I) [4] Hereditary fructose intolerance [5] Lowe syndrome [6] Tyrosinemia Wilson's [ipfs.io]

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Combined Oxidative Phosphorylation Defect Type 14

storage disease due to aldolase A deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to lactate dehydrogenase [csbg.cnb.csic.es]

Disease Type Ib 3 Glycogen Storage Disease Type Ic 3 Glycogen Storage Disease Type II 10 Glycogen Storage Disease Type III 5 Glycogen Storage Disease Type IV 4 Glycogen Storage [preventiongenetics.com]

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Secondary Myopathy

Neuropathy Some Glycogen storage diseases Parasitic polymyositis Pyomyositis a.k.a. [learningneurology.com]

storage disease (E74.0) lipid storage disorders (E75.-) Information for Patients Muscle Disorders Also called: Myopathy Your muscles help you move and help your body work [icdlist.com]

GSD Type II (Pompc's Disease / Acid Maltase Deficiency - AMD) Type II Glycogen Storage Disease is an inborn error of metabolism that belongs to a group called lysosomal storage [annalsofneurosciences.org]

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Hyperuricemia

To identify the mechanism of hyperuricemia in glycogen storage diseases (glycogenoses) that affect muscle, we studied the effects of exercise and prolonged rest on purine [ncbi.nlm.nih.gov]

Glycogen storage diseases, especially type I, III, V, and VII, also cause hyperuricemia. [hindawi.com]

Crofford, 2008 8 Hyperuricemic Syndromes: Pathophysiology and Therapy Glycogen Storage Diseases Hyperuricemia and typical clinical gout occur in teenagers and adults with [educalingo.com]

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