CLSI Announces Guidelines for Newborn Screening for Cystic Fibrosis
The abbreviated Wilson and Jungner criteria1 for an inheritable disorder to be considered for testing include an acceptable prevalence in the population, serious medical complications if not treated before symptoms arise, the potential for successful treatment, the availability of technology to scre...
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Veröffentlicht in: | Laboratory medicine 2012-05, Vol.43 (4), p.31-32 |
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description | The abbreviated Wilson and Jungner criteria1 for an inheritable disorder to be considered for testing include an acceptable prevalence in the population, serious medical complications if not treated before symptoms arise, the potential for successful treatment, the availability of technology to screen hundreds of specimens daily, and cost favorability (ie, the cost of detection by screening is significantly less than a clinical diagnosis). Newborn screening for cystic fibrosis (CF) meets these requirements and has been included in the 30 core disorders, recommended by the US Secretary of Health and Human Services, for which all state newborn screening programs should screen. |
doi_str_mv | 10.1309/LM2AIVMAI9TR6JQI |
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Newborn screening for cystic fibrosis (CF) meets these requirements and has been included in the 30 core disorders, recommended by the US Secretary of Health and Human Services, for which all state newborn screening programs should screen.</description><subject>Babies</subject><subject>Colleges & universities</subject><subject>Committees</subject><subject>Cystic fibrosis</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Medical screening</subject><subject>Mutation</subject><subject>Newborn babies</subject><subject>Public health</subject><subject>Quality 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universities</topic><topic>Committees</topic><topic>Cystic fibrosis</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Medical screening</topic><topic>Mutation</topic><topic>Newborn babies</topic><topic>Public health</topic><topic>Quality control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoffman, Gary L</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni 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Newborn screening for cystic fibrosis (CF) meets these requirements and has been included in the 30 core disorders, recommended by the US Secretary of Health and Human Services, for which all state newborn screening programs should screen.</abstract><cop>Chicago</cop><pub>Oxford University Press</pub><doi>10.1309/LM2AIVMAI9TR6JQI</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Babies Colleges & universities Committees Cystic fibrosis Deoxyribonucleic acid DNA Medical screening Mutation Newborn babies Public health Quality control |
title | CLSI Announces Guidelines for Newborn Screening for Cystic Fibrosis |
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