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Multiple carboxylase deficiency
Results: 20

#	Item
1	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet Add to Reading List Source URL: www.babysfirsttest.org Language: English - Date: 2012-11-09 11:16:32 Genodermatoses Holocarboxylase synthetase deficiency Multiple carboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Newborn screening Biotinidase deficiency 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Biotin Medical genetics Medicine Health Pediatrics
2	2007 Newborn Screening Standards in Georgia (specifically methylmalonic acidemia) Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2011-08-22 14:09:02 Newborn screening Methylmalonic acidemia Multiple carboxylase deficiency Isovaleric acidemia Methylmalonic acid Hyperammonemia Organic acidemia Maple syrup urine disease Biotinidase deficiency Health Rare diseases Medicine
3	Biotinidase Deficiency (BlOT) (metabolic condition: organic acid disorder) Also known as: • BTD deficiency How is BlOT treated? Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:30:59 B vitamins Biotinidase deficiency Genes Biotinidase Biotin Multiple carboxylase deficiency Medical genetics 3-Methylcrotonyl-CoA carboxylase deficiency Holocarboxylase synthetase deficiency Medicine Genetics Health
4	Microsoft Word - HCSD update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-06-21 19:39:54 Genodermatoses Holocarboxylase synthetase deficiency Holocarboxylase synthetase Rare diseases Multiple carboxylase deficiency Biotin Newborn screening Genetic testing Health Medicine Genetics
5	Biotinidase Deficiency Biotinidase deficiency is an autosomal recessive inherited disorder that results in the inability to process the vitamin biotin in the normal way. Early symptoms of biotinidase deficiency generally Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:37:29 Biotinidase deficiency Biotinidase Biotin Newborn screening Multiple carboxylase deficiency Holocarboxylase synthetase deficiency Health Genetics Genetic genealogy
6	NEWBORN SCREENING FACT SHEET HCSD or MCD Holocarboxylase Synthetase Deficiency Multiple Carboxylase Deficiency – Neonatal (MCD) What is it? HCSD stands for holocarboxylase synthetase Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:57 Genes Genodermatoses Holocarboxylase synthetase deficiency Holocarboxylase synthetase Biotin Multiple carboxylase deficiency Newborn screening Health Genetics Medicine
7	Biotinidase Deficiency What problems can Biotinidase Deficiency cause? What is a positive newborn screen? Newborn screening is done on tiny samples of Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 21:07:49 Medicine Biotinidase deficiency Biotinidase Biotin Newborn screening Biotin deficiency Multiple carboxylase deficiency Health Genetics B vitamins
8	Minnesota Department of Health[removed]POSITIVE NEWBORN SCREEN Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:16 Medicine Biotinidase Biotin Newborn screening Multiple carboxylase deficiency Biotin deficiency Health Genetics Biotinidase deficiency
9	2012 Minnesota Department of Health POSITIVE NEWBORN SCREEN Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:08 Medicine Biotinidase Newborn screening Biotin Multiple carboxylase deficiency Biotin deficiency Health Genetics Biotinidase deficiency
10	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