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Propionic acidemia
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#	Item
91	Parent Fact Sheet DISORDER Methylmalonic Acidemia (Cbl A, B) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have problems Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 01:32:54 Genetic genealogy Vitamin B12 Methylmalonic acidemia Methylmalonic acid Acidosis Protein Propionic acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Rare diseases
92	Organic Acid Disorders Information for Parents  Overview Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2013-09-05 15:51:36 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Organic acidemia Beta-ketothiolase deficiency Multiple carboxylase deficiency Health Rare diseases Genetic genealogy
93	Microsoft Word - 35 PS 621 et seq _2_.doc Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-07-10 11:10:50 Genetic genealogy Newborn screening Maple syrup urine disease Phenylketonuria Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Galactosemia Biotinidase deficiency Health Medicine Rare diseases
94	Microsoft Word - Current News on Expanded Newborn Screening[removed]doc Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 07:17:02 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Inborn error of lipid metabolism Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
95	Parent Fact Sheet DISORDER Methylmalonic Acidemia Mutase Deficiency (MUT) CAUSE MMA stands for "methylmalonic acidemia". It is one type of organic acid disorder. People with MMA have Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 03:31:10 Genetic genealogy Methylmalonic acidemia Vitamin B12 Acidosis Methylmalonic acid Protein Propionic acidemia Glutaric aciduria type 1 Health Medicine Rare diseases
96	Rhode Island screens babies for 28 health conditions and hearing loss. The conditions are grouped in the categories explained below, and a list of all the conditions is on the other side of this card. Early detection and Add to Reading List Source URL: health.ri.gov Language: English - Date: 2014-06-27 15:48:15 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Biotinidase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Biotin Health Rare diseases Genetic genealogy
97	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:47:40 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Fatty-acid metabolism disorder 3-Methylcrotonyl-CoA carboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
98	NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:51 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Health Rare diseases Genetic genealogy
99	OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:54 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
100	Microsoft Word - MoD Fact Sheet 2011 Add to Reading List Source URL: azdhs.gov Language: English - Date: 2012-04-12 12:46:55 Medical genetics Newborn screening Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Health Rare diseases Genetic genealogy

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