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

Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide.

Forensic science international - 15 Jul 2011

Eminoglu Tuba F, Tumer Leyla, Okur Ilyas, Ezgu Fatih S, Biberoglu Gursel, Hasanoglu Alev

Abstract excerpt

Very-long-chain acyl-coenzyme A (CoA) dehydrogenase deficiency (VLCADD) (OMIM #201475) is an autosomal recessive disorder of fatty acid oxidation. Major phenotypic expressions are hypoketotic hypoglycemia, hepatomegaly, cardiomyopathy, myopathy, rhabdomyolysis, elevated creatinine kinase, and lipid infiltration of liver and muscle. At the same time, it is a rare cause of Sudden Infant Death Syndrome (SIDS) or...

Read the complete abstract on PubMed

Topics

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

Share to Acyl-CoA Dehydrogenase, Long-Chain
Share to Congenital Bone Marrow Failure Syndromes

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Forensic Genetics

Share to Heart Septal Defects

Share to Hypertrophy, Left Ventricular

Share to Lipid Metabolism, Inborn Errors

Share to Metabolism, Inborn Errors

Share to Muscular Diseases

Source

Identifiers

PMID: 21531094
DOI: 10.1016/j.forsciint.2011.04.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide.PMID 21531094Read ↗

Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotype.Semantic proximity Read ↗

Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card.Semantic proximity Read ↗

Rare Korean Cases of Very-long-chain Acyl-CoA Dehydrogenase Deficiency with a Novel Recurrent Mutation.Semantic proximity Read ↗

[Clinical features and ACADVL gene mutation spectrum analysis of 11 Chinese patients with very long chain acyl-CoA dehydrogenase deficiency].Semantic proximity Read ↗

Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening.Semantic proximity Read ↗

Positive newborn screen in a normal infant of a mother with asymptomatic very long-chain Acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Medium-chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman.Semantic proximity Read ↗

Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected sibling.Semantic proximity Read ↗

Molecular diagnosis for a fatal case of very long-chain acyl-CoA dehydrogenase deficiency in Hong Kong Chinese with a novel mutation: a preventable death by newborn screening.Semantic proximity Read ↗

Molecular and clinical characteristics of very-long-chain acyl-CoA dehydrogenase deficiency: A single-center experience in Saudi Arabia.Semantic proximity Read ↗

Late-onset multiple acyl-CoA dehydrogenase deficiency: an insidious presentation.Semantic proximity Read ↗

The diagnostic challenge in very-long chain acyl-CoA dehydrogenase deficiency (VLCADD).Semantic proximity Read ↗

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