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Fatty-acid metabolism disorder / Carnitine-acylcarnitine translocase deficiency / Carnitine / Newborn screening / Health / Rare diseases / Medicine


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
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Document Date: 2007-09-13 15:09:34

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Company

FOD (Fatty Oxidation Disorder) Family Support Group / /

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Facility

University Hospital / Hospital St. Louis / American College of Medical Genetics Newborn Screening ACT Sheets / Children’s Mercy Hospital / Cardinal Glennon Children’s Hospital / /

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IndustryTerm

elevated chemicals / food / energy / /

MedicalCondition

fatty acid oxidation disorders / inherited fatty acid oxidation disorder / coma / Carnitine/Acylcarnitine Translocase Deficiency / autosomal recessive disorder / cardiac arrest / rare fatty acid oxidation disorder / metabolic disorders / hypoglycemia / Fatty Oxidation Disorder / /

Movie

What is it? / /

Organization

Children’s Mercy Hospital Kansas City / American College of Medical Genetics Newborn Screening ACT Sheets / St. Louis Children’s Hospital St. Louis / University Hospital / United Mitochondrial Disease Foundation / Department of Health / Save Babies Through Screening Foundation / /

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Position

care physician / physician / /

ProgrammingLanguage

php / /

ProvinceOrState

Pennsylvania / /

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http / /

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http /

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