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Medical genetics / Organic acidemia / Isovaleric acidemia / Propionic acidemia / Newborn screening / Methylmalonic acidemia / Glutaric aciduria type 1 / Malonyl-CoA decarboxylase deficiency / 3-Methylcrotonyl-CoA carboxylase deficiency / Health / Rare diseases / Genetic genealogy


(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD)
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Document Date: 2007-05-01 10:03:12

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File Size: 21,87 KB

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Country

United States / Saudi Arabia / Canada / /

Currency

MGA / /

IndustryTerm

carrier frequency / carrier testing / energy / /

MedicalCondition

chronic intermittent form presents / cerebral palsy / specific disorder / intercurrent illness / mental retardation / CoA Lyase deficiency / CoA Dehydrogenase deficiency / cardiomyopathy / hypocalcemia / suspected disorder / acidosis / seizures / soft neurologic signs / metabolic acidosis / acute encephalopathy / coma / cerebral hemorrhage / neutropenia / specific disorders / nephritis / organic acid disorder / thrombocytopenia / CoA Hydratase deficiency / ketoacidotic coma / hypotonia / lactic acidosis / truncal hypotonia / fever / Isobutyryl CoA Dehydrogenase deficiency / lethargy / ketosis / vomiting / movement disorders / encephalopathy / hyper/hypoglycemia / rare disorders / pancreatitis / severe metabolic acidosis / disorder / osteoporosis / infection / hypotonia / dystonia / hypoglycemia / chronic form / neurologic symptoms / disorders / pancytopenia / CoA Carboxyl deficiency / dehydration / /

MedicalTreatment

low protein diet / Low-protein diet / Liver transplant / antibiotic therapy / /

Organization

Vanderbilt University School of Medicine Definition / /

Person

John A Phillips / Marilee Weingartner / /

Product

glycine / /

ProvinceOrState

Pennsylvania / /

Technology

diagnostic tests / genotype / /

SocialTag