An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders

Screening newborns using genome sequencing is being explored due to its potential to expand the list of conditions that can be screened. Previously, we proposed the need for large-scale pilot studies to assess the feasibility of screening highly penetrant genetic neurodevelopmental disorders. Here,...

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Bibliographic Details
Main Authors: Wendy K. Chung (Author), Stephen M. Kanne (Author), Zhanzhi Hu (Author)
Format: Book
Published: MDPI AG, 2024-04-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Wendy K. Chung  |e author 
700 1 0 |a Stephen M. Kanne  |e author 
700 1 0 |a Zhanzhi Hu  |e author 
245 0 0 |a An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders 
260 |b MDPI AG,   |c 2024-04-01T00:00:00Z. 
500 |a 10.3390/ijns10020033 
500 |a 2409-515X 
520 |a Screening newborns using genome sequencing is being explored due to its potential to expand the list of conditions that can be screened. Previously, we proposed the need for large-scale pilot studies to assess the feasibility of screening highly penetrant genetic neurodevelopmental disorders. Here, we discuss the initial experience from the GUARDIAN study and the systemic gaps in clinical services that were identified in the early stages of the pilot study. 
546 |a EN 
690 |a newborn screening (NBS) 
690 |a genome sequencing (GS) 
690 |a neurodevelopmental disorder (NDD) 
690 |a variants of unknown significance (VUS) 
690 |a early intervention program (EIP) 
690 |a genomic uniform screening against rare diseases in all newborns (GUARDIAN) 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n International Journal of Neonatal Screening, Vol 10, Iss 2, p 33 (2024) 
787 0 |n https://www.mdpi.com/2409-515X/10/2/33 
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