11![Microsoft Word - CAT_update_2013 Microsoft Word - CAT_update_2013](https://www.pdfsearch.io/img/6d9e481e77e02b2ac0297a0deee043e8.jpg) | Add to Reading ListSource URL: www.newbornscreening.infoLanguage: English - Date: 2013-12-01 02:16:23
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12![NEWBORN SCREENING FACT SHEET CPT-2 Deficiency (Carnitine Palmitoyl Transferase Deficiency, CACT, Type 2) in infancy. Most people do not have symptoms until their teen years or early adulthood. This is called classic form NEWBORN SCREENING FACT SHEET CPT-2 Deficiency (Carnitine Palmitoyl Transferase Deficiency, CACT, Type 2) in infancy. Most people do not have symptoms until their teen years or early adulthood. This is called classic form](https://www.pdfsearch.io/img/766df55c77a65a659786a1f5d6e7cbcd.jpg) | Add to Reading ListSource URL: www.ndhealth.govLanguage: English - Date: 2009-02-19 11:31:59
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13![NEWBORN SCREENING FACT SHEET LCHADD (Long Chain 3-Hydroxyacyl-CoA Dehydrogenese Deficiency) What is it? LCHADD stands for long chain 3-hydroxyacylCoA dehydrogenase deficiency. It is one type of fatty acid oxidation disor NEWBORN SCREENING FACT SHEET LCHADD (Long Chain 3-Hydroxyacyl-CoA Dehydrogenese Deficiency) What is it? LCHADD stands for long chain 3-hydroxyacylCoA dehydrogenase deficiency. It is one type of fatty acid oxidation disor](https://www.pdfsearch.io/img/32fc4e4fd23d4766d9a2be34c910a5fb.jpg) | Add to Reading ListSource URL: www.ndhealth.govLanguage: English - Date: 2009-02-19 11:31:59
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14![` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the ` NEWBORN SCREENING FACT SHEET VLCADD (Very Long Chain Acyl-CoA Dehydrogenese Deficiency) It is common for babies and children with the](https://www.pdfsearch.io/img/e87c682d4d1dbfdbcdd84a566b04c58d.jpg) | Add to Reading ListSource URL: www.ndhealth.govLanguage: English - Date: 2009-02-19 11:32:01
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15![Disease Name CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY (CACT) (SOLUTE CARRIER FAMILY 25 (CARNITINE/ACYLCARNITINE TRANSLOCASE), MEMBER 20; CARNITINE-ACYLCARNITINE CARRIER; CACT DEFICIENCY) Fatty acid oxidation defect Disease Name CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY (CACT) (SOLUTE CARRIER FAMILY 25 (CARNITINE/ACYLCARNITINE TRANSLOCASE), MEMBER 20; CARNITINE-ACYLCARNITINE CARRIER; CACT DEFICIENCY) Fatty acid oxidation defect](https://www.pdfsearch.io/img/0d68c67c3133172bcbf00a02832fc718.jpg) | Add to Reading ListSource URL: www.idph.state.ia.usLanguage: English - Date: 2007-06-25 16:35:55
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16![Microsoft Word - cpt2_ref Microsoft Word - cpt2_ref](https://www.pdfsearch.io/img/5e4f8d821ab302ccc32a765b44df8d4d.jpg) | Add to Reading ListSource URL: www.idph.state.ia.usLanguage: English - Date: 2007-06-25 16:36:03
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17![Microsoft Word - CPT2_update_2013 Microsoft Word - CPT2_update_2013](https://www.pdfsearch.io/img/9e306621b623955404880e7ac861b7ea.jpg) | Add to Reading ListSource URL: www.newbornscreening.infoLanguage: English - Date: 2013-12-01 02:35:36
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18![Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria Disorders Detected By Mississippi Genetic Newborn Screening Secondary Conditions Methylmalonic acidemia with homocystinuria Malonic acidemia Isobutyrylglycinuria](https://www.pdfsearch.io/img/4f4c70cb42975861922fba305c0f76e6.jpg) | Add to Reading ListSource URL: msdh.ms.govLanguage: English - Date: 2012-03-28 12:35:21
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19![Microsoft Word - CPT2 update, 2011.doc Microsoft Word - CPT2 update, 2011.doc](https://www.pdfsearch.io/img/f047fe85298aa6f3804c97efde77abcb.jpg) | Add to Reading ListSource URL: www.newbornscreening.infoLanguage: English - Date: 2011-05-26 16:26:05
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20![Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. Patient Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. Patient](https://www.pdfsearch.io/img/865cfc4fc6d7dd3f55496344a1b77a6e.jpg) | Add to Reading ListSource URL: www.health.mo.govLanguage: English - Date: 2007-09-13 15:09:34
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