TECHNICAL REPORT Newborn Screening Fact Sheets Celia I. Kaye, MD, PhD, and the Committee on Genetics Abbreviations: OMIM, Online Mendelian Inheritance in Man; MS MS, tandem mass spectrometry; CoA, coenzyme A; BTD, bioti - 21-Hydroxylase - Document - PDFSEARCH.IO

First Page		Document Content
Date: 2010-07-29 16:02:48 Adrenal gland disorders Intersexuality Deafness Mental retardation Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital adrenal hyperplasia Newborn screening Biotinidase deficiency Congenital hearing loss Health Medicine Pediatrics		TECHNICAL REPORT Newborn Screening Fact Sheets Celia I. Kaye, MD, PhD, and the Committee on Genetics Abbreviations: OMIM, Online Mendelian Inheritance in Man; MS/MS, tandem mass spectrometry; CoA, coenzyme A; BTD, bioti Add to Reading List Source URL: www.idph.state.ia.us Download Document from Source Website File Size: 227,76 KB Share Document on Facebook

	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial DocID: 14zTU - View Document
	Newborn Screening Year in Review 86,586 For Babies Born in 2013 Bloodspot Samples Received Initial DocID: 11G3r - View Document
	Chart of Metabolic Disorders Screened Table of Disorders Screened by Program Condition Incidence DocID: Z5KR - View Document
	American College of Medical Genetics ACT SHEET Newborn Screening ACT Sheet DocID: Ri0X - View Document
	CYTOGENETIC STUDIES ROUTINE AND HIGH RESOLUTION BLOOD Collect 4-6 mls of peripheral blood in a green top sodium heparin tube. Please do not used lithium heparin or ammonium heparin as these can be toxic to the cells. Tra DocID: O1GM - View Document