Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency.
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| Title: | Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency. |
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| Authors: | Chen T; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Sun MQ; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Xu F; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Hao LL; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Liang LL; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Zhang KC; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Yang Y; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Sun YN; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Wang RF; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Gu XF; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China., Huang YL; Guangzhou Newborn Screening Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China., Zou H; Neonatal Disease Screening Center, Jinan Maternity and Child Health Hospital Affiliated to Shandong First Medical University, Jinan, China., Zhu BS; Department of Medical Genetics, NHC Key Laboratory of Preconception Health Birth in Western China, The First People's Hospital of Yunnan Province, Affiliated Hospital of Kunming University of Science and Technology, Kunming, China., Wang XH; Department of Genetics, Inner Mongolia Maternity and Child Health Care Hospital, Hohhot, China., Miao JK; Department of Pediatrics, Chongqing Health Center for Women and Children & Women and Children's Hospital of Chongqing Medical University, Chongqing, China., Feng JZ; Department of Genetics, Shijiazhuang Maternal and Child Health Hospital, Shijiazhuang, China., Huang CD; Neonatal Disease Screening Center, Hainan Women and Children's Medical Center, Haikou, China., Fan CN; BGI Genomics, BGI-Shenzhen, Shenzhen, China., Qiu WJ; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China. qiuwenjuan@xinhuamed.com.cn., Han LS; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China. hanlianshu@xinhuamed.com.cn. |
| Source: | World journal of pediatrics : WJP [World J Pediatr] 2026 May; Vol. 22 (5), pp. 596-601. Date of Electronic Publication: 2026 May 29. |
| Publication Type: | Letter |
| Journal Info: | Publisher: Springer International Publ Country of Publication: Switzerland NLM ID: 101278599 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1867-0687 (Electronic) NLM ISO Abbreviation: World J Pediatr Subsets: MEDLINE; In Process |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42215828 AccessLevel: 2 PubType: Editorial & Opinion PubTypeId: editorialOpinion PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Chen+T%22">Chen T</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Sun+MQ%22">Sun MQ</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Xu+F%22">Xu F</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Hao+LL%22">Hao LL</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Liang+LL%22">Liang LL</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Zhang+KC%22">Zhang KC</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Yang+Y%22">Yang Y</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Sun+YN%22">Sun YN</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Wang+RF%22">Wang RF</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Gu+XF%22">Gu XF</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.<br /><searchLink fieldCode="AU" term="%22Huang+YL%22">Huang YL</searchLink>; Guangzhou Newborn Screening Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.<br /><searchLink fieldCode="AU" term="%22Zou+H%22">Zou H</searchLink>; Neonatal Disease Screening Center, Jinan Maternity and Child Health Hospital Affiliated to Shandong First Medical University, Jinan, China.<br /><searchLink fieldCode="AU" term="%22Zhu+BS%22">Zhu BS</searchLink>; Department of Medical Genetics, NHC Key Laboratory of Preconception Health Birth in Western China, The First People's Hospital of Yunnan Province, Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.<br /><searchLink fieldCode="AU" term="%22Wang+XH%22">Wang XH</searchLink>; Department of Genetics, Inner Mongolia Maternity and Child Health Care Hospital, Hohhot, China.<br /><searchLink fieldCode="AU" term="%22Miao+JK%22">Miao JK</searchLink>; Department of Pediatrics, Chongqing Health Center for Women and Children & Women and Children's Hospital of Chongqing Medical University, Chongqing, China.<br /><searchLink fieldCode="AU" term="%22Feng+JZ%22">Feng JZ</searchLink>; Department of Genetics, Shijiazhuang Maternal and Child Health Hospital, Shijiazhuang, China.<br /><searchLink fieldCode="AU" term="%22Huang+CD%22">Huang CD</searchLink>; Neonatal Disease Screening Center, Hainan Women and Children's Medical Center, Haikou, China.<br /><searchLink fieldCode="AU" term="%22Fan+CN%22">Fan CN</searchLink>; BGI Genomics, BGI-Shenzhen, Shenzhen, China.<br /><searchLink fieldCode="AU" term="%22Qiu+WJ%22">Qiu WJ</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China. qiuwenjuan@xinhuamed.com.cn.<br /><searchLink fieldCode="AU" term="%22Han+LS%22">Han LS</searchLink>; Department of Pediatric Endocrinology and Genetic, Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China. hanlianshu@xinhuamed.com.cn. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101278599%22">World journal of pediatrics : WJP</searchLink> [World J Pediatr] 2026 May; Vol. 22 (5), pp. 596-601. <i>Date of Electronic Publication: </i>2026 May 29. – Name: TypePub Label: Publication Type Group: TypPub Data: Letter – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer+International+Publ%22">Springer International Publ </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101278599 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1867-0687 (Electronic) <i>NLM ISO Abbreviation: </i>World J Pediatr <i>Subsets: </i>MEDLINE; In Process |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42215828 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s12519-026-01032-7 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 596 Titles: – TitleFull: Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Chen T – PersonEntity: Name: NameFull: Sun MQ – PersonEntity: Name: NameFull: Xu F – PersonEntity: Name: NameFull: Hao LL – PersonEntity: Name: NameFull: Liang LL – PersonEntity: Name: NameFull: Zhang KC – PersonEntity: Name: NameFull: Yang Y – PersonEntity: Name: NameFull: Sun YN – PersonEntity: Name: NameFull: Wang RF – PersonEntity: Name: NameFull: Gu XF – PersonEntity: Name: NameFull: Huang YL – PersonEntity: Name: NameFull: Zou H – PersonEntity: Name: NameFull: Zhu BS – PersonEntity: Name: NameFull: Wang XH – PersonEntity: Name: NameFull: Miao JK – PersonEntity: Name: NameFull: Feng JZ – PersonEntity: Name: NameFull: Huang CD – PersonEntity: Name: NameFull: Fan CN – PersonEntity: Name: NameFull: Qiu WJ – PersonEntity: Name: NameFull: Han LS IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2026 May Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1867-0687 Numbering: – Type: volume Value: 22 – Type: issue Value: 5 Titles: – TitleFull: World journal of pediatrics : WJP Type: main |
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