221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

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221 newborn-screened neonates with medium-chain acyl-coenzyme A dehydrogenase deficiency: Findings from the Inborn Errors of Metabolism Collaborative

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作者：Kristi Bentler^a ; Shaohui Zhai^b ; Sara A. Elsbecker^c ; Georgianne L. Arnold^d ; Barbara K. Burton^e ; Jerry Vockley^d ; Cynthia A. Cameron^b ; Sally J. Hiner^b ; Mathew J. Edick^b ; Susan A. Berry^c ; ¹ ; ² ; ^{berry002@umn.edu" class="auth_mail" title="E-mail the corresponding author} ; On behalf of the Inborn Errors of Metabolism CollaborativeJanet Thomas^g ; Melinda Dodge^g ; Rani Singh^h ; Sangeetha Lakshman^h ; Katie Coakley^h ; Adrya Stembridge^h ; Alvaro Serrano Russiⁱ ; Emily Phillipsⁱ ; Barbara Burton^j ; Clare Edano^j ; Sheela Shrestha^j ; George Hoganson ; Lauren Dwyer^k ; Bryan Hainline^l ; Susan Romie^l ; Sarah Hainline^l ; Alexander Asamoah^m ; Kara Goodin^m ; Cecilia Rajakaruna^m ; Kelly Jackson^m ; Ada Hamoshⁿ ; Hilary Vernonⁿ ; Nancy Smithⁿ ; Ayesha Ahmad^o ; Sue Lipinski^o ; Gerald Feldman^p ; Susan Berry^q ; Sara Elsbecker^q ; Kristi Bentler^r ; Esperanza Font-Montgomery^s ; Dawn Peck^s ; Loren D.M. Pena^t ; Dwight D. Koeberl^t ; Yong-hui Jiang^t ; Priya S. Kishnani^t ; William Rizzo^u ; Machelle Dawson^u ; Nancy Ambrose^u ; Paul Levy^v ; David Kronn^w ; Chin-to Fong^x ; Kristin D&rsquo ; Aco^x ; Theresa Hart^x ; Richard Erbe^y ; Melissa Samons^y ; Nancy Leslie^z ; Racheal Powers^z ; Dennis Bartholomew^aa ; Melanie Goff^aa ; Sandy vanCalcar^ab ; Joyanna Hansen^ab ; Georgianne Arnold^ac ; Jerry Vockley^ac ; Cate Walsh-Vockley^ad ; William Rhead^ad ; David Dimmock^ad ; Paula Engelking^ad ; Cassie Bird^ad ; Ashley Swan^ad ; Jessica Scott Schwoerer^ae ; Sonja Henry^ae ; TaraChandra Narumanchi^af ; Marybeth Hummel^af ; Jennie Wilkins^af ; Laura Davis-Keppen^ag ; Quinn Stein^ag ; Rebecca Loman^ag ; Cynthia Cameron^ah ; Mathew J. Edick^ah ; Sally J. Hiner^ah ; Kaitlin Justice^ah ; Shaohui Zhai^ah
关键词：Medium-chain acyl-coenzyme A dehydrogenase deficiency ; MCAD ; Octanoylcarnitine ; ACADM ; Newborn screening ; Inborn error of metabolism
刊名：Molecular Genetics and Metabolism
出版年：2016
出版时间：September-October 2016
年：2016
卷：119
期：1-2
页码：75-82
全文大小：271 K

文摘

•: Retrospective analysis of 221 newborn-screened subjects with MCAD deficiency
•: NBS C8 and genotype were significant predictors of having neonatal symptoms.
•: Symptomatic neonates were more likely to have at least one copy of 985A > G mutation.
•: Neonates with select triggers were more likely to have symptoms.
•: The IBEM-IS is a platform to better understand newborn-screened conditions.

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