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Holocarboxylase synthetase deficiency
Results: 24

#	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	Microsoft Word - Biotinidase_Deficiency_fact_sheet_for_web_2003_doc.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-04-15 07:49:08 Biotinidase deficiency Biotinidase Biotin Genetic disorder Medical genetics Biotin deficiency Holocarboxylase synthetase deficiency Medicine Genetics Health
3	Biotinidase Deficiency Jewell C. Ward, MD, Ph D, Chief, Division of Medical Genetics Department of Pediatrics University of Tennessee-Memphis 711 Jefferson, CDD, Room 522 Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:01:52 Biotinidase deficiency Genes Biotinidase Biocytin Biotin Newborn screening Medical genetics Biotin deficiency Holocarboxylase synthetase deficiency Medicine Health Genetics
4	Microsoft Word - Biotinidase_Deficiency.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:40:55 Biotinidase Genetic genealogy Medical genetics Biotin Biotin deficiency Holocarboxylase synthetase deficiency Genetics Genes Biotinidase deficiency
5	Parents‛ Guide To BD Biotinidase Deficiency California Department of Public Health Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:50 Genetics Genes Biotinidase deficiency Biotinidase Biotin Newborn screening Vitamin Biotin deficiency Holocarboxylase synthetase deficiency B vitamins Health Nutrition
6	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
7	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
8	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
9	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
10	NEWBORN SCREENING FACT SHEET HMG Lyase Deficiency (3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency) If HMG lyase deficiency is not treated, what problems occur? Each child with HMG lyase deficiency will Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:58 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Newborn screening Biotin 3-hydroxy-3-methylglutaryl-CoA lyase Holocarboxylase synthetase Health Genetics Medicine