Disease Name SHORT-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (SCADD) (ACADS DEFICIENCY; SCADH DEFICIENCY; SCAD DEFICIENCY) Fatty acid oxidation defect Classification: Inheritance:

First Page		Document Content
Date: 2007-06-25 16:37:49 Chemistry Metabolism Fatty acids Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology ACADS Malonyl-CoA decarboxylase deficiency Newborn screening Health Medicine Rare diseases		Disease Name SHORT-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (SCADD) (ACADS DEFICIENCY; SCADH DEFICIENCY; SCAD DEFICIENCY) Fatty acid oxidation defect Classification: Inheritance: Add to Reading List Source URL: www.idph.state.ia.us Download Document from Source Website File Size: 23,64 KB Share Document on Facebook

	POSTER SESSIONS The LIPID MAPS meeting features two poster sessions with 44 posters. Of these, twelve were selected for lightning talks (see program) by the review committee, consisting of Susan A. Henry, Alfred H. Merri DocID: 19Ufx - View Document
	What is Carnitine ? Nelson LS Tang, MBChB, FRCPA Associate Professor Department of Chemical Pathology The Chinese University of Hong Kong DocID: 13Fs6 - View Document
	Timeliness of Newborn Screening – DACHDNC’s laboratory standards and procedures subcommittee draft findings DocID: 12jOC - View Document
	Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence DocID: Z5KR - View Document
	Disorders and Reference Ranges DocID: KTuv - View Document