NORD - National Organization For Rare Disorders, Inc. glutaricaciduria I. To purchase fulltext report ($7.50) Copyright 1987, 1990,1994, 2004 Synonyms of glutaricaciduria I Dicarboxylic Aminoaciduria; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Glutaricacidu
Conditions And Diseases - Glutaricaciduria Top Links Related Healthcare Subjects. Disabilities, Environmental Health, Fitness, Health Insurance, Healthcare Industry, Medicine, Men's Health. glutaricaciduria Web Site Links. Glutaric Aciduria Type 1 Information and links for children with GA1. message board and links. NORD - glutaricaciduria I - Offers alternate names, a http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
NORD - National Organization For Rare Disorders, Inc. glutaricaciduria II. Copyright 1987, 1988, 1990, 1992, 1997, 2004 Synonymsof glutaricaciduria II Electron Transfer Flavoprotein, Deficiency of; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Glutaricacidu
Glutaricaciduria Fatty Oxdiation Disorders. Galactosemia. glutaricaciduria. Mineral Metabolism Disorders. Leigh's Disease links for children with GA1. NORD glutaricaciduria I - http//www.stepstn.com http://www.medlina.com/glutaricaciduria.htm
Glutaricaciduria - Information / Diagnosis / Treatment / Prevention home genetic disorders glutaricaciduria glutaricaciduria. NORD glutaricaciduriaI Offers alternate names, a general discussion and resources. http://www.healthcyclopedia.com/genetic-disorders/glutaricaciduria.html
Extractions: Web Directory: Glutaric Aciduria Type 1 Information and links for children with GA1. IOGA: International Organization of Glutaric Acidemia Information about the organization, their services and about the disease. Including events, newsletter, FAQs, message board and links. NORD: Glutaricaciduria I Offers alternate names, a general discussion and resources.
Glutaricaciduria I glutaricaciduria is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutarylCoA dehydrogenase. One of a group of disorders known as "organic acidemias " it is Babies http://hw.healthdialog.com/kbase/nord/nord383.htm
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: Glutaricaciduria is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. One of a group of disorders known as "organic acidemias," it is characterized by decreased muscle tone (hypotonia), vomiting, and excess acid in the blood. Affected individuals may also have involuntary movements of the trunk and limbs (dystonia or athetosis) and mental retardation may also occur. Babies with Glutaricaciduria usually appear normal at birth. During the first year of life decreased muscle tone (hypotonia), vomiting, and acidity of the blood may occur. Taking on strange positions due to disordered muscle tone (dystonia), involuntary and ceaseless slow, sinuous, writhing (athetotic) or jerky (choreic) movements of the trunk and limbs may also occur in combination with mental retardation.
Disease Directory : Genetic Disorders : Glutaricaciduria Antenatal diagnosis of glutaricaciduria type II. Antenatal diagnosisof glutaricaciduria type II. glutaricaciduria - glutaricaciduria. http://www.diseasedirectory.net/Genetic_Disorders/Glutaricaciduria/default.aspx
Extractions: Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Glutaricaciduria Antenatal diagnosis of glutaricaciduria type II. - Antenatal diagnosis of glutaricaciduria type II. Mitchell G, Saudubray JM, Benoit Y, Rocchiccioli F, Charpentier C, Ogier H, Boue J. Publication Types: CLASSIFIEDS.TERADEX.COM - Health/Fitness/Diseases/Genetic ... - CLASSIFIEDS.TERADEX.COM - Health/Fitness/Diseases/Genetic Disorders/Glutaricaciduria. Ad-Space.net Banner Network. Aaex.com, Aaex.com, Conditions and Diseases: Genetic Disorders: Glutaricaciduria ... Dominion Web Directory - /Health/Conditions_and_Diseases ... - Top: Health: Conditions_and_Diseases: Genetic_Disorders: Glutaricaciduria: Glutaricaciduria (4). Click here to visit our sponsor. See also: electricbrain home: index: Health: Conditions and Diseases ... - Famous quotes: With the news that Nancy Reagan has referred to an astrologer when planning her husband's schedule, and reports of Genetic Disorders / Glutaricaciduria - Genetic Disorders / Glutaricaciduria. Categories related to Glutaricaciduria: Glutaric Aciduria Type 1 - Information and links for children with GA1.
AllRefer Health Health Links Directory Conditions And Diseases .com Health Health Directory Conditions and Diseases Genetic Disorders glutaricaciduria (4 NORD glutaricaciduria I. Offers alternate names, a general discussion and resources http://www.1uphealth.com/links/genetic-disorders-glutaricaciduria.html
Glutaricaciduria II glutaricaciduria II Important It is possible that the main title ofthe report glutaricaciduria II is not the name you expected. http://my.webmd.com/hw/raising_a_family/nord378.asp
Extractions: 1) Glutaricaciduria IIA (GA IIA), Neonatal Form of Glutaricaciduria II. This neonatal form of Glutaricaciduria II is a very rare, sex-linked hereditary disorder characterized by large amounts of glutaric and other acids in blood and urine. Some researchers believe the disorder is caused by a defect in the breakdown of acyl-CoA compounds.
Glutaricaciduria I glutaricaciduria I Important It is possible that the main title of thereport glutaricaciduria I is not the name you expected. Please http://my.webmd.com/hw/raising_a_family/nord383.asp
Extractions: Glutaricaciduria is a rare hereditary metabolic disorder, caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase. One of a group of disorders known as "organic acidemias," it is characterized by decreased muscle tone (hypotonia), vomiting, and excess acid in the blood. Affected individuals may also have involuntary movements of the trunk and limbs (dystonia or athetosis) and mental retardation may also occur. Resources
Cardiac + Myopathy; Cardiomyopathy Multiple acylCoA dehydrogenase deficiency (MADD; glutaricaciduria IIA) l Electron transfer flavoprotein, http://www.neuro.wustl.edu/neuromuscular/msys/cardiac.html
Extractions: Carnitine Distribution: 90% in muscle Fatty acids are transported from cytoplasm to mitochondria Mitochondrial oxidation of fatty acids provides energy source Chief energy sources for: Prolonged fasting; Skeletal muscle during exercise; Cardiac muscle Types of deficiency Loss of carnitine results in Clinical features: General Specific enzyme defects can include
Extractions: Links about Glutaricaciduria Glutaric Aciduria Type 1 - Information and links for children with GA1. IOGA: International Organization of Glutaric Acidemia - Information about the organization, their services and about the disease. Including events, newsletter, FAQs, message board and links. Pediatric Database - A definition of glutaric aciduria, epidemiology, pathogenesis, clinical features, investigations and management.
Health Library - glutaricaciduria I. glutaricaciduria is a rare hereditary metabolic disorder,caused by a deficiency of the enzyme glutarylCoA dehydrogenase. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw
Health Library - glutaricaciduria II. Important It is possible that the main title ofthe report glutaricaciduria II is not the name you expected. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw
Glutaricaciduria II glutaricaciduria II. General Discussion. There are two forms of glutaricaciduriaII which occur during different stages of life. They http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord378
Glutaricaciduria II There are two forms of glutaricaciduria II which occur during differentstages of life. They urine. 1) glutaricaciduria IIA (GA. http://www.bchealthguide.org/kbase/nord/nord378.htm
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: There are two forms of Glutaricaciduria II which occur during different stages of life. They are both forms of organic acidemias which are a group of metabolic disorders characterized by excess acid in the blood and urine. 1) Glutaricaciduria IIA (GA IIA), Neonatal Form of Glutaricaciduria II. This neonatal form of Glutaricaciduria II is a very rare, sex-linked hereditary disorder characterized by large amounts of glutaric and other acids in blood and urine. Some researchers believe the disorder is caused by a defect in the breakdown of acyl-CoA compounds.
Non Ketotic Hyperglycinemia (For more information on this disorder, choose Methylmalonic Acidemia as yoursearch term in the Rare Disease Database.) glutaricaciduria II (Glutaric http://www.bchealthguide.org/kbase/nord/nord520.htm
Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: Non-Ketotic Hyperglycinemia is a genetic disorder characterized by an error of amino acid metabolism. Large amounts of the amino acid glycine tend to accumulate in body fluids particularly in the cerebrospinal fluid. The metabolic block occurs in the conversion of glycine into smaller molecules. Severe illness usually occurs soon after birth and many patients become mentally retarded and/or develop seizure disorders. Non-Ketotic Hyperglycinemia is characterized early in life by severe illness, failure to thrive, low muscle tone (hypotonia), and drowsiness or lethargy. Mental retardation may develop, relatively mild in some cases, but usually severe. Seizures, usually with jerking motions (myoclonus) may also occur. The amount of glycine in blood, urine and cerebrospinal fluid is extremely high.
Swiss-Prot Keyword: Glutaricaciduria Genetic Disorders, glutaricaciduria Submit Your Site to the glutaricaciduria category. Sponsored glutaricaciduriaSites. Submit Your Site to the glutaricaciduria category. Sponsored Results. http://ca.expasy.org/cgi-bin/get-entries?KW=Glutaricaciduria
