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![]() Date: 2012-11-09 11:16:32Genodermatoses 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 | Add to Reading List |
![]() | American College of Medical Genetics ACT SHEET Newborn Screening ACT SheetDocID: Ri0X - View Document |
![]() | 2007 Newborn Screening Standards in Georgia (specifically methylmalonic acidemia)DocID: EO9W - View Document |
![]() | Biotinidase Deficiency (BlOT) (metabolic condition: organic acid disorder) Also known as: • BTD deficiency How is BlOT treated?DocID: E2ue - View Document |
![]() | Microsoft Word - HCSD update 2011.docDocID: E1Gb - View Document |
![]() | 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 generallyDocID: D0kS - View Document |