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Methylcrotonyl-CoA
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#	Item
11	Maine Newborn Screening Program List of Conditions Each baby born in Maine is screened for the conditions listed below. This list is correct as of July 1, 2008 but may change as conditions are added to or removed from th Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:14 Medical genetics Newborn screening Hyperammonemia 3-Methylcrotonyl-CoA carboxylase deficiency Isovaleric acidemia Glutaric acidemia type 2 Glutaric aciduria type 1 Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
12	NEWBORN SCREENING FACT SHEET 3MCC Deficiency (3-Methylcrotonyl CoA Carboxylase Deficiency) 3MCC deficiency can cause episodes of illness called metabolic crises. Some of the first symptoms of a metabolic crisis are: Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:55 Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Biotinidase deficiency Biotin deficiency Health Genetic genealogy Medical genetics
13	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:06 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylcrotonyl-CoA carboxylase Propionic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
14	Microsoft Word - Rhode Island insert Khmer.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:33 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Mitochondrial trifunctional protein deficiency Methylcrotonyl-CoA 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
15	Effect of Supplemental Biotin on Performance of Lactating Dairy Cows1 Bill Weiss Department of Animal Sciences Ohio Agricultural Research and Development Center The Ohio State University, Wooster 44691 Add to Reading List Source URL: dairy.osu.edu Language: English - Date: 2011-05-26 10:27:43 Biology Biotin deficiency Biotin Propionyl-CoA carboxylase Pyruvate carboxylase Milk Vitamin Methylcrotonyl-CoA carboxylase Acetyl-CoA carboxylase Chemistry Nutrition B vitamins
16	Overview of Newborn Screening for Biotinidase Deficiency – For Parents What is newborn screening? What are the symptoms of biotinidase deficiency? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:40 Medicine Biotinidase Biotin Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Biotin deficiency Health Genetics Biotinidase deficiency
17	Microsoft Word - Vermont Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2008-04-01 13:39:57 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
18	Overview of Newborn Screening for 3-MCC Deficiency – For Parents What is newborn screening? What are the symptoms of 3-MCC deficiency? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:41 Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Biotinidase deficiency Isobutyryl-coenzyme A dehydrogenase deficiency Health Genetic genealogy Medical genetics
19	Title 15 - Mississippi Department of Health Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2014-03-27 09:48:48 Newborn screening Congenital adrenal hyperplasia Galactosemia Phenylketonuria Biotinidase deficiency Congenital hypothyroidism 3-Methylcrotonyl-CoA carboxylase deficiency Inborn error of metabolism 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
20	Microsoft Word - 3MCC_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-11-28 02:14:59 Rare diseases 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Methylcrotonyl-CoA carboxylase Biotinidase deficiency Biotin deficiency Health Genetic genealogy Medical genetics