Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency.

Saved in:
Bibliographic Details
Title: Combined biochemical and genetic analysis improves early diagnosis and prenatal assessment of multiple acyl-CoA dehydrogenase deficiency.
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
Description
ISSN:1867-0687
DOI:10.1007/s12519-026-01032-7