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category genetic or congenital, metabolic frequency rare (U.S.) Usually seen in children.

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long chain fatty acyl dehydrogenase (lcad) deficiency - inherited disorder of fat metabolism Definition for long chain fatty acyl dehydrogenase (LCAD) deficiency some common symptoms delayed development not gaining weight poor appetite vomiting some related diagnoses 1 - 7 of 316 diagnoses hyponatremia cystic fibrosis hypercalcemia hyperoxaluria common variable immunodeficiency viral gastroenteritis alcoholism   more do i have 'long chain fatty acyl dehydrogenase (LCAD) deficiency'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'long chain fatty acyl dehydrogenase (lcad) deficiency' 1 - 4 of 4 diagnostic tests urine Organic Acids long chain fatty acyl dehydrogenase (LCAD) deficiency and urine Organic Acids Urine chromatography long chain fatty acyl dehydrogenase (LCAD) deficiency and Urine chromatography Serum Organic Acids long chain fatty acyl dehydrogenase (LCAD) deficiency and Serum Organic Acids urine pH long chain fatty acyl dehydrogenase (LCAD) deficiency and urine pH therapeutic procedures for 'long chain fatty acyl dehydrogenase (LCAD) deficiency'? 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 long chain fatty acyl dehydrogenase (LCAD) deficiency: therapeutic procedure search results for 'long chain fatty acyl dehydrogenase (lcad) deficiency' rankings are computer generated. please consult your health care provider. medications search results for 'long chain fatty acyl dehydrogenase (lcad) deficiency' rankings are computer generated. please consult your health care provider. web search results for long chain fatty acyl dehydrogenase (lcad) deficiency Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - long chain fatty acyl dehydrogenase (LCAD) deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency ... Medium-chain acyl-coenzyme A dehydrogenase deficiency is a fatty acid ... The length of the fatty acids chains can vary; they may be classified as very long-chain, ... http://en.wikipedia.org/wiki/Medium-chain_acyl-coenzyme_A_de...   en.wikipedia.org - summary LCAD DEFICIENCY - Pedbase.org LCAD is one of four ezymes in the mitochondria responsible for the breakdown of long-chain (C12-C18) fatty ... the accumulation of long-chain acyl-CoA intermediates within the ... http://www.pedbase.org/l/lcad-deficiency/   www.pedbase.org - summary Autosomal Deletion Syndromes Medium Chain Co-A Acyl-Dehydrogenase Deficiency ? Prototype for FAO disorders ... Long chain/very long chain acyl CoA dehydrogenase deficiency (LCAD, VLCAD) ... http://www.cdc.gov/nchs/ppt/icd9/att4_1203.ppt   www.cdc.gov - summary Acadl - NextBio Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia. [ provided by RefSeq] ... http://www.nextbio.com/b/search/ov/Acadl?type=feature   www.nextbio.com - summary LCAD(Acadl) - NextBio catalyzes the alpha, beta-dehydrogenation of acyl-CoA esters in fatty acid metabolism [RGD] http://www.nextbio.com/b/search/ov/LCAD   www.nextbio.com - summary SCAD DEFICIENCY - Pedbase.org there are 3 straight-chain acyl-CoA dehydrogenases to deal with long, medium, and short chain fatty acids. LCAD, MCAD, and SCAD are all homotetramers ... http://www.pedbase.org/s/scad-deficiency/   www.pedbase.org - summary Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD ... ImportantIt is possible that the main title of the report Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)is not the name you expected. http://health.yahoo.com/children-genetic/very-long-chain-acy...   health.yahoo.com - summary Newborn screening - Wikipedia, the free encyclopedia Long-chain hydroxyacyl-CoA dehydrogenase deficiency (LCHAD) > 1 in 75, ... chain acyl-CoA dehydrogenase deficiency (MCAD) > 1 in 25,000. Very-long-chain acyl-CoA dehydrogenase ... http://en.wikipedia.org/wiki/Newborn_screening   en.wikipedia.org - summary ICD-9-CM Coordination and Maintenance Committee Meeting ... peroxisomes are involved in the metabolism of very long chain fatty acids. ... Long chain/very long chain acyl CoA dehydrogenase. deficiency (LCAD, ... http://www.cdc.gov/nchs/data/icd9/agendadec03.pdf   www.cdc.gov - summary AAT (alpha-1 antitrypsin) deficiency 273 LCAD (long chain/very long chain acyl CoA dehydrogenase deficiency, VLCAD) ... LCHAD (long chain 3-hydroxyacyl CoA dehydrogenase deficiency) 277.85 ... http://www.cdc.gov/nchs/data/icd9/icdidx_addenda05.pdf   www.cdc.gov - summary 1 TABULAR ADDENDA OCTOBER 1, 2004 (FY05) Long chain/very long chain acyl CoA dehydrogenase. deficiency (LCAD, VLCAD) Medium chain ... Short chain acyl CoA dehydrogenase deficiency (SCAD) Excludes: ... http://www.cdc.gov/nchs/data/icd9/icdtab_addenda05.pdf   www.cdc.gov - summary show more 1