Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Screening for newborn fatty acid oxidation disorders in Chongqing and the follow-up of confirmed children.

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences - 25 Jun 2022

Chen Min, Yin Yifan, Liu Hao, Peng Yong, Ye Liang, Luo Qian, Miao Jingkun

Abstract excerpt

OBJECTIVE: To investigate the incidence, clinical characteristics, gene mutations and prognosis of fatty acid oxidation disorders (FAOD) in newborns in Chongqing. METHODS: Blood samples were collected from 35 374 newborns for screening of FAOD in the Neonatal Screening Center of Women and Children's Hospital of Chongqing Medical University from July 2020 to February 2022. The acylcarnitine spectrum was detected...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carnitine
Share to Fatty Acids

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Infant, Newborn

Share to Lipid Metabolism, Inborn Errors

Share to Mutation

Share to Neonatal Screening

Share to Solute Carrier Family 22 Member 5

Source

Open in PubMed Open full text

Identifiers

PMID: 36207828
DOI: 10.3724/zdxbyxb-2022-0218
PMCID: PMC9511477

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening for newborn fatty acid oxidation disorders in Chongqing and the follow-up of confirmed children.PMID 36207828Read ↗

Newborn screening for fatty acid oxidation disorders: epidemiological and genetic findings in Southeastern China.Semantic proximity Read ↗

Spectrum Analysis of Inherited Metabolic Disorders for Expanded Newborn Screening in a Central Chinese PopulationSemantic proximity Read ↗

Screening and follow-up results of neonate medium-chain acyl-CoA dehydrogenase deficiency in Zibo, Shandong province.Semantic proximity Read ↗

[Screening and genetic variation analysis of fatty acid oxidation disorder in neonates in Qingdao City].Semantic proximity Read ↗

Biochemical And Genetic Characteristics of Patients With Primary Carnitine Deficiency Identified Through Newborn ScreeningSemantic proximity Read ↗

Clinical, Biochemical and Molecular Characterisation of Newborns With Fatty Acid β-Oxidation Disorders: Novel Variants in the ACADM , ACADVL and SLC22A5 Genes.Semantic proximity Read ↗

Newborn screening and genetic variation of medium chain acyl-CoA dehydrogenase deficiency in the Chinese population.Semantic proximity Read ↗

Screening of multiple acyl-CoA dehydrogenase deficiency in newborns and follow-up of patients.Semantic proximity Read ↗

Biochemical and genetic characteristics of patients with primary carnitine deficiency identified through newborn screening.Semantic proximity Read ↗

[Newborn screening for primary carnitine deficiency and variant spectrum of SLC22A5 gene in Guangzhou].Semantic proximity Read ↗

Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis.Semantic proximity Read ↗

Newborn screening and molecular features of patients with multiple acyl-CoA dehydrogenase deficiency in Quanzhou, China.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.