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

A series of pregnancies in women with inherited metabolic disease

14 Sept 2011

Abstract excerpt

In this case series we report 12 pregnancies, in women treated at four centres, illustrating some of the issues that may be encountered during pregnancy by women with inherited metabolic disease. We discuss how specific pregnancy, labour and delivery issues for mothers with methylmalonic acidemia, homocystinuria, propionic acidemia, glutaric acidemia type 1, ornithine transcarbamylase (OTC) deficiency and...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Enzymes and Metabolism
Share to Folate and B Vitamins Research
Share to Metabolism and Genetic Disorders

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

Source

Identifiers

PMID: 21918856
DOI: 10.1007/s10545-011-9389-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 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

A series of pregnancies in women with inherited metabolic diseasePMID 21918856Read ↗

Pregnancy issues in inherited metabolic disordersSemantic proximity Read ↗

Propionic acidemia: a Turkish case report of a successful pregnancy, labor and lactation.Semantic proximity Read ↗

One-carbon metabolism enzyme polymorphisms and uteroplacental insufficiency.Semantic proximity Read ↗

Three successful pregnancies through dietary management of fructose-1,6-bisphosphatase deficiency.Semantic proximity Read ↗

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complicationsSemantic proximity Read ↗

Gaucher's disease and pregnancy.Semantic proximity Read ↗

Liver disease in pregnancy and fetal fatty acid oxidation defects.Semantic proximity Read ↗

Treatment of cobalamin C (cblC) deficiency during pregnancy.Semantic proximity Read ↗

Mitochondrial fatty acid transport enzyme deficiency--implications for in vitro fertilization.Semantic proximity Read ↗

Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency†Semantic proximity Read ↗

Myotonic dystrophy and pregnancy.Semantic proximity Read ↗

Pregnancy of a patient with multiple Acyl-CoA dehydrogenation deficiency (MADD).Semantic proximity Read ↗

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