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glycogen storage diseases - type of storage disease due to accumulation of glycogen in tissues Definition for glycogen storage diseases Glycogen storage disease (synonyms: glycogenosis, dextrinosis) is any one of several inborn errors of metabolism that result from enzyme defects that affect the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types. There are nine diseases that are commonly considered to be glycogen storage diseases: some common symptoms bodyache fatigue stomach swelling weakness some related diagnoses 1 - 7 of 128 diagnoses hypokalemic periodic paralysis periodic paralyses variegate porphyria hyperkalemic periodic paralysis metabolic alkalosis hyponatremia hyperkalemia   more do i have 'glycogen storage diseases'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'glycogen storage diseases' 1 - 5 of 58 diagnostic tests Molecular Genetic Studies glycogen storage diseases and Molecular Genetic Studies Muscle biopsy glycogen storage diseases and Muscle biopsy Phosphorylase b kinase in skeletal muscle glycogen storage diseases and Phosphorylase b kinase in skeletal muscle Phosphorylase b kinase in the liver glycogen storage diseases and Phosphorylase b kinase in the liver muscle phosphorylase glycogen storage diseases and muscle phosphorylase Abdominal CAT Scan glycogen storage diseases and Abdominal CAT Scan Abdominal MRI MRI of abdominal contents glycogen storage diseases and Abdominal MRI Arterial Blood Gas glycogen storage diseases and Arterial Blood Gas BUN glycogen storage diseases and BUN Carcinoembryonic Antigen (CEA) glycogen storage diseases and Carcinoembryonic Antigen (CEA) Complete Blood Count glycogen storage diseases and Complete Blood Count Complete metabolic panel glycogen storage diseases and Complete metabolic panel ECHOcardiogram glycogen storage diseases and ECHOcardiogram EKG Electrocardiogram glycogen storage diseases and EKG Electromyogram (EMG) glycogen storage diseases and Electromyogram (EMG) Hepatic ultrasonography glycogen storage diseases and Hepatic ultrasonography Liver Function Tests elevated liver enzymes glycogen storage diseases and Liver Function Tests Plasma uric acid glycogen storage diseases and Plasma uric acid Prothrombin Time (PT) glycogen storage diseases and Prothrombin Time (PT) Reticulocyte count glycogen storage diseases and Reticulocyte count Serum Alkaline Phosphatase (ALP) glycogen storage diseases and Serum Alkaline Phosphatase (ALP) Serum Creatinine glycogen storage diseases and Serum Creatinine Serum Lactate glycogen storage diseases and Serum Lactate Serum alpha-fetoprotein (AFP) glycogen storage diseases and Serum alpha-fetoprotein (AFP) Ultrasonography kidneys ureter bladder glycogen storage diseases and Ultrasonography kidneys ureter bladder fasting lipid profile glycogen storage diseases and fasting lipid profile serum glucose glycogen storage diseases and serum glucose urine amino acids glycogen storage diseases and urine amino acids Amniocentesis glycogen storage diseases and Amniocentesis Biopsy liver glycogen storage diseases and Biopsy liver Chorionic Villus Sampling (CVS) glycogen storage diseases and Chorionic Villus Sampling (CVS) Forearm ischemic exercise test glycogen storage diseases and Forearm ischemic exercise test Oral Glucose Tolerance Test glycogen storage diseases and Oral Glucose Tolerance Test oral amino acids and proteins load test glycogen storage diseases and oral amino acids and proteins load test oral galactose and fructose tests glycogen storage diseases and oral galactose and fructose tests oral glucagon and epinephrine tests glycogen storage diseases and oral glucagon and epinephrine tests hepatic phosphorylase in the liver glycogen storage diseases and hepatic phosphorylase in the liver serum hypoxanthine glycogen storage diseases and serum hypoxanthine serum inosine glycogen storage diseases and serum inosine MRI with phosphate-31 glycogen storage diseases and MRI with phosphate-31 Magnetic Resonance Imaging (MRI) Spectroscopy procedure to determine structure of molecules glycogen storage diseases and Magnetic Resonance Imaging (MRI) Spectroscopy Phosphorylase b kinase in heart glycogen storage diseases and Phosphorylase b kinase in heart Activated partial thromboplastin time glycogen storage diseases and Activated partial thromboplastin time Nerve conduction studies (NCS) glycogen storage diseases and Nerve conduction studies (NCS) Serum ammonia glycogen storage diseases and Serum ammonia Serum calcium glycogen storage diseases and Serum calcium Serum phosphorus glycogen storage diseases and Serum phosphorus Total bilirubin glycogen storage diseases and Total bilirubin Urinalysis Examination of urine to detect disease glycogen storage diseases and Urinalysis direct bilirubin glycogen storage diseases and direct bilirubin Lipoprotein Electrophoresis glycogen storage diseases and Lipoprotein Electrophoresis Lipoprotein Phenotyping glycogen storage diseases and Lipoprotein Phenotyping Periodic acid-Schiff (PAS) staining glycogen storage diseases and Periodic acid-Schiff (PAS) staining Serum Triglyceride Triglyceride Test glycogen storage diseases and Serum Triglyceride Urinary ketones glycogen storage diseases and Urinary ketones Urinary oligosaccharides glycogen storage diseases and Urinary oligosaccharides serum electrolytes glycogen storage diseases and serum electrolytes tandem mass spectrometry glycogen storage diseases and tandem mass spectrometry for more please login, login is free (click to login) therapeutic procedures for 'glycogen storage diseases'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for glycogen storage diseases: therapeutic procedure search results for 'glycogen storage diseases' 1 - 2 of 2 therapeutic procedures rankings are computer generated. please consult your health care provider. Liver Transplant Replacing diseased liver by healthy one glycogen storage diseases and Liver Transplant Enzyme replacement glycogen storage diseases and Enzyme replacement medications search results for 'glycogen storage diseases' 1 - 5 of 9 medications rankings are computer generated. please consult your health care provider.   Glucagon glycogen storage diseases and Glucagon   Allopurinol glycogen storage diseases and Allopurinol   Captopril glycogen storage diseases and Captopril   Enalapril glycogen storage diseases and Enalapril   Alglucosidase alfa glycogen storage diseases and Alglucosidase alfa   Lisinopril glycogen storage diseases and Lisinopril   Ramipril glycogen storage diseases and Ramipril   Ferrous sulfate glycogen storage diseases and Ferrous sulfate   Filgrastim glycogen storage diseases and Filgrastim for more please login, login is free (click to login) web search results for glycogen storage diseases Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - glycogen storage diseases Nutritional therapy for glycogen storage diseases. Nutritional therapy for glycogen storage diseases. Heller S, Worona L, Consuelo A. ... Glycogen storage diseases (GSDs) are a group of inherited disorders ... http://www.ncbi.nlm.nih.gov/pubmed/18667910?ordinalpos=2&ito   www.ncbi.nlm.nih.gov - summary The hepatic glycogen storage diseases--problems beyond childhood. The hepatic glycogen storage diseases--problems beyond childhood. Lee PJ, Leonard JV. ... the prognosis for patients with the hepatic glycogen storage diseases. ... http://www.ncbi.nlm.nih.gov/pubmed/7494404   www.ncbi.nlm.nih.gov - summary Glycogen storage disease type V - Wikipedia, the free encyclopedia Glycogen storage disease type V (GSD-V) is a metabolic disorder, more ... metabolism disorders (including glycogen storage diseases) (E73-74, 271) ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_V   en.wikipedia.org - summary Glycogen storage disease type IV - Wikipedia, the free encyclopedia Glycogen storage disease type IV. From Wikipedia, the free encyclopedia ... metabolism disorders (including glycogen storage diseases) (E73-74, 271) ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_IV   en.wikipedia.org - summary Glycogen storage disease type VI - Wikipedia, the free encyclopedia Glycogen storage disease type VI. From Wikipedia, the free encyclopedia ... metabolism disorders (including glycogen storage diseases) (E73-74, 271) ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_VI   en.wikipedia.org - summary Glycogen Storage Disease Type I - Yahoo! Health Important It is possible that the main title of the report Glycogen Storage Disease Type I is not the name you expected. Please check the synonyms listing to find ... http://health.yahoo.com/digestive-overview/glycogen-storage-...   health.yahoo.com - summary Glycogen storage disease type I - Wikipedia, the free encyclopedia Glycogen storage disease type I has an autosomal recessive pattern of inheritance. ... Chen Y-T, Burchell A. Glycogen storage diseases. ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_I   en.wikipedia.org - summary Carbohydrate Metabolism: Hereditary Metabolic Disorders: Merck Manual ... Glycogen Storage Diseases. Galactosemia. Hereditary Fructose Intolerance. Back to Top ... Glycogen storage diseases tend to cause uric acid, a waste product, to ... http://www.merck.com/mmhe/sec23/ch282/ch282b.html   www.merck.com - summary Glycogen Storage Disease VIII - Yahoo! Health Important It is possible that the main title of the report Glycogen Storage Disease VIII is not the name you expected. Please check the synonyms listing to find the ... http://health.yahoo.com/digestive-overview/glycogen-storage-...   health.yahoo.com - summary Glycogen storage disease type III - Wikipedia, the free encyclopedia Glycogen storage disease type III is an autosomal recessive metabolic disorder ... metabolism disorders (including glycogen storage diseases) (E73-74, 271) ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_III   en.wikipedia.org - summary Glycogen storage disease type 0 - Wikipedia, the free encyclopedia Glycogen storage disease type 0 is characterized by a deficiency in the glycogen ... metabolism disorders (including glycogen storage diseases) (E73-74, 271) ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_0   en.wikipedia.org - summary Glycogen Storage Disease Type V - Yahoo! Health Important It is possible that the main title of the report Glycogen Storage Disease Type V is not the name you expected. Please check the synonyms listing to find ... http://health.yahoo.com/other-other/glycogen-storage-disease...   health.yahoo.com - summary Glycogen storage disease type III (glycogen debranching enzyme ... PATIENTS: All patients with glycogen storage disease type III who were followed ... Glycogen Storage Disease Type III/complications. Humans. Immunoblotting ... http://www.ncbi.nlm.nih.gov/pubmed/1580445   www.ncbi.nlm.nih.gov - summary Glycogen storage disease type IX - Wikipedia, the free encyclopedia Glycogen storage disease type IX. From Wikipedia, the free encyclopedia ... metabolism disorders (including glycogen storage diseases) (E73-74, 271) ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_IX   en.wikipedia.org - summary Carbohydrate Metabolism Disorders: Inherited Disorders of Metabolism ... Inheritance for glycogen storage diseases (GSDs) is autosomal recessive except ... Glycogen Storage Diseases and Disorders of Gluconeogenesis ... http://www.merck.com/mmpe/sec19/ch296/ch296d.html   www.merck.com - summary Glycogen storage disease type II: clinical overview. Glycogen storage disease type II: clinical overview. Di Rocco M, Buzzi D, Tarò M. ... Glycogen storage disease type II has a broad continuous clinical spectrum in ... http://www.ncbi.nlm.nih.gov/pubmed/17915568   www.ncbi.nlm.nih.gov - summary McArdle syndrome Glycogen storage disease type V (GSDV); Myophosphorylase deficiency; Muscle ... resources, visit the Association for Glycogen Storage Disease at www.agsdus.org. ... http://adam.about.com/HIE/000329.htm   adam.about.com - summary Neonatal type IV glycogen storage disease associated with "null ... ... neonatal form of type IV glycogen storage disease (GSD IV) was diagnosed on ... Storage Disease Type IV/pathology* Humans. Infant, Newborn. Liver Diseases ... http://www.ncbi.nlm.nih.gov/pubmed/15520786   www.ncbi.nlm.nih.gov - summary WebMD Health A-Z - Find reliable health and medical information on ... Glycogen Disease of Muscle Type VII. Glycogen Storage ... Glycogen Storage Disease VIII. Glycogenosis Type I. Glycogenosis Type II. Glycogenosis Type III ... http://www.webmd.com/a-to-z-guides/health-topics/gk-go.htm   www.webmd.com - summary Glycogen storage disease - Wikipedia, the free encyclopedia glycogen storage disease at Dorland's Medical Dictionary ... a b "eMedicine - Glycogen-Storage Disease Type VI : Article by Lynne Ierardi-Curto" ... http://en.wikipedia.org/wiki/Glycogen_storage_disease   en.wikipedia.org - summary Pompe disease - Genetics Home Reference Gene Review: Glycogen Storage Disease Type II (Pompe Disease) ... Glycogen Storage Disease Type II. GSD II. Lysosomal alpha-1,4-glucosidase deficiency ... http://ghr.nlm.nih.gov/condition=pompedisease   ghr.nlm.nih.gov - summary Glycogen storage disease type II - Wikipedia, the free encyclopedia It is the only glycogen storage disease with a defect in lysosomal metabolism, ... "eMedicine - Glycogen-Storage Disease Type II : Article by Jennifer Ibrahim" ... http://en.wikipedia.org/wiki/Glycogen_storage_disease_type_II   en.wikipedia.org - summary Index: GL: Merck Manual Home Edition Glycogen. Carbohydrates, Proteins, and Fats: Carbohydrates. storage diseases of (glycogenoses) Disorders of Carbohydrate Metabolism: Glycogen Storage Diseases ... http://www.merck.com/mmhe/index/ind_gl.html   www.merck.com - summary Von Gierke disease Association for Glycogen Storage Disease -- www.agsdus.org. Outlook (Prognosis) ... There is no simple way to prevent glycogen storage disease. ... http://adam.about.com/HIE/000338trt.htm   adam.about.com - summary Fetal type IV glycogen storage disease: clinical, enzymatic, and ... Fetal type IV glycogen storage disease: clinical, enzymatic, and genetic data of ... Glycogen Storage Disease Type IV/physiopathology* Humans. Male. Pregnancy ... http://www.ncbi.nlm.nih.gov/pubmed/16278887   www.ncbi.nlm.nih.gov - summary 2008 MeSH Tree Structures. C18 - Nutritional and Metabolic Diseases Glycogen Storage Disease Type II [C18.452.132.100.435.340] ... Storage Diseases, Nervous ... Glycogen Storage Disease Type I [C18.452.648.202.449.448] ... http://www.nlm.nih.gov/mesh/trees2008/C18.html   www.nlm.nih.gov - summary Glycogen - Wikipedia, the free encyclopedia These are collectively referred to as glycogen storage diseases. [edit] Synthesis ... Glycogen storage disease - McArdle's Disease Website. MeSH Glycogen. v ? d ? e ... http://en.wikipedia.org/wiki/Glycogen   en.wikipedia.org - summary Orphanet: Glycogen storage disease type 2 The portal for rare diseases and orphan drugs ... Glycogen storage disease type 2. Orpha number. ORPHA365. Prevalence of rare diseases ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=365   www.orpha.net - summary Hers Disease - Yahoo! Health ... is possible that the main title of the report Hers Disease is not the name you expected. Please check the synonyms ... as the glycogen storage disorders. ... http://health.yahoo.com/blood-overview/hers-disease/healthwise--nord401.html   health.yahoo.com - summary Introduction: Muscular Dystrophies and Related Disorders: Merck Manual ... ... include congenital myopathies, periodic paralysis, and glycogen storage diseases. Glycogen storage diseases are a group of rare inherited disorders in which ... http://www.merck.com/mmhe/print/sec05/ch073/ch073a.html   www.merck.com - summary Mutation frequencies for glycogen storage disease Ia in the Ashkenazi ... Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population. ... Glycogen storage disease type Ia (GSDIa) is a severe autosomal recessive ... http://www.ncbi.nlm.nih.gov/pubmed/15316959   www.ncbi.nlm.nih.gov - summary Search Results Glycogen Storage Diseases Glycogen storage diseases are caused by deficiencies ... to get there faster: Go Fa Fabry's disease Lysosomal Storage Disorders: Fabry's. ... http://www.merck.com/mrksearch/SearchServlet?filtN=professio...   www.merck.com - summary Orphanet: Glycogen storage disease type 4 The portal for rare diseases and orphan drugs ... It is evident that glycogen storage disease type IV exists in multiple forms ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=367   www.orpha.net - summary Glycogen synthase (GYS1) mutation causes a novel skeletal muscle ... It is unlike glycogen storage diseases resulting from known defects in ... Glycogen Storage Disease/enzymology. Glycogen Storage Disease/genetics ... http://www.ncbi.nlm.nih.gov/pubmed/18358695?ordinalpos=3&ito...   www.ncbi.nlm.nih.gov - summary MedlinePlus: Liver Diseases Genetics Home Reference: Cholesteryl ester storage disease(National Library of Medicine) ... Type I Glycogen Storage Disease(American Liver Foundation) ... http://www.nlm.nih.gov/medlineplus/liverdiseasesgeneral.html   www.nlm.nih.gov - summary Encyclopedia G-Gz on Yahoo! Health Health encyclopedia of diseases and conditions covering symptoms, ... Glycogen Storage Disease. Glycogen Storage Disease Type V. Glycogen Storage Disease VIII ... http://health.yahoo.com/ency/g/   health.yahoo.com - summary Glycogen Breakdown and Synthesis Are Reciprocally Regulated A Biochemical Understanding of Glycogen-Storage Diseases Is Possible Edgar von ... Seven other glycogen-storage diseases have been characterized ( Table 21.1 ) ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?db=Books&rid=stryer.section.2955   www.ncbi.nlm.nih.gov - summary Forbes Disease - Yahoo! Health ... is possible that the main title of the report Forbes Disease is not the name you expected. Please check the synonyms ... several glycogen storage disorders ... http://health.yahoo.com/other-other/forbes-disease/healthwise--nord396.html   health.yahoo.com - summary PubMed Link Image ... cycle enzyme defects resembles that seen in glycogen storage disease but can be ... metabolism Glycogen metabolism Glycogen Storage Disease diagnosis diet ... http://www.ncbi.nlm.nih.gov/pubmed/15795597   www.ncbi.nlm.nih.gov - summary Orphanet: Glycogen storage disease type 3 The portal for rare diseases and orphan drugs ... Glycogen storage disease type III (Cori's or Forbes' disease) is caused by the ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=366   www.orpha.net - summary Polysaccharide storage myopathy in canine phosphofructokinase ... ... in canine phosphofructokinase deficiency (type VII glycogen storage disease) ... Glycogen Storage Disease Type VII/pathology. Glycogen Storage Disease Type ... http://www.ncbi.nlm.nih.gov/pubmed/2137952   www.ncbi.nlm.nih.gov - summary THE MERCK MANUAL--SECOND HOME EDITION, Types and Characteristics of ... The Merck Manual of Medical Information--Second Home Edition http://www.merck.com/mrkshared/mmanual_home2/tb/tb282_1.jsp   www.merck.com - summary Lysosomal storage disease - Wikipedia, the free encyclopedia Lysosomal storage diseases (LSDs) (pronounced l?s??s?m?l ) are a group of ... Beta-mannosidosis. Pompe disease/Glycogen storage disease type II. Pycnodysostosis ... http://en.wikipedia.org/wiki/Lysosomal_storage_disease   en.wikipedia.org - summary Orphanet: Glycogen storage disease type 7 The portal for rare diseases and orphan drugs ... Glycogen storage disease type VII (Tarui's disease) is rare as it has only been ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=371   www.orpha.net - summary Laboratory diagnosis of lysosomal storage diseases Introduction Lysosomal storage diseases (LSDs) represent a heterogeneous group ... fucosidosis, a -mannosidosis and glycogen storage disease type II. Urinary ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?indexed=google&rid=fabry.chapter.556   www.ncbi.nlm.nih.gov - summary List of diseases (G) - Wikipedia, the free encyclopedia Glycogen storage disease type 1D. Glycogen storage disease type 6, due to phosphorylation ... Glycogen storage disease type V. Glycogen storage disease type VI ... http://en.wikipedia.org/wiki/List_of_diseases_(G)   en.wikipedia.org - summary Recombinant human acid alpha-glucosidase enzyme therapy for infantile ... PURPOSE: Infantile glycogen storage disease type II (GSD-II) is a fatal genetic ... Glycogen/metabolism. Glycogen Storage Disease Type II/therapy* Heart/physiology ... http://www.ncbi.nlm.nih.gov/pubmed/11286229   www.ncbi.nlm.nih.gov - summary Glycogen Storage Disease Type VII - Yahoo! Health Important It is possible that the main title of the report Glycogen Storage Disease Type VII is not the name you expected. Please check the synonyms listing to find ... http://health.yahoo.com/children-genetic/glycogen-storage-di...   health.yahoo.com - summary Orphanet: Glycogen storage disease due to LAMP 2 deficiency The portal for rare diseases and orphan drugs ... Glycogen storage disease due to LAMP-2 (Lysosomal-Associated Membrane Protein 2) ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=34587   www.orpha.net - summary Pompe's disease. Pompe's disease, glycogen-storage disease type II, and acid maltase deficiency ... Disease Progression. Genotype. Glycogen Storage Disease Type II*/diagnosis ... http://www.ncbi.nlm.nih.gov/pubmed/18929906?ordinalpos=1&ito...   www.ncbi.nlm.nih.gov - summary show more 1  2