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Biotin deficiency
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11	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
12	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Genetics Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Biotinidase deficiency Biotinidase Galactosemia Biotin Congenital adrenal hyperplasia Health Medicine Pediatrics
13	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Epidemiology Newborn screening Pediatrics Inborn errors of carbohydrate metabolism Biotinidase deficiency Galactosemia Biotinidase Biotin Blood Health Medicine Biology
14	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Genetics Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Biotinidase deficiency Biotinidase Galactosemia Amino acid Biotin Health Medicine Pediatrics
15	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
16	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Genetics Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Biotinidase deficiency Biotinidase Galactosemia Biotin Congenital adrenal hyperplasia Health Medicine Pediatrics
17	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:08 Epidemiology Newborn screening Pediatrics Inborn errors of carbohydrate metabolism Biotinidase deficiency Biotinidase Galactosemia Biotin C16 Health Genetics Medicine
18	Microsoft Word - Chart_of_Table_of_Metabolic_Disorders_rev.doc Add to Reading List Source URL: health.hawaii.gov Language: English - Date: 2013-05-30 20:03:03 Rare diseases Fatty-acid metabolism disorder Glutaric aciduria type 1 Very long-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Biotinidase deficiency Biotin Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Medicine Genetic genealogy
19	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
20	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

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