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

P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.

Current opinion in pediatrics - 1 Aug 2006

Flück Christa E, Miller Walter L

Abstract excerpt

PURPOSE OF REVIEW: P450 oxidoreductase deficiency--a newly described form of congenital adrenal hyperplasia--typically presents a steroid profile suggesting combined deficiencies of steroid 21-hydroxylase and 17alpha-hydroxylase/17,20-lyase activities. These and other enzymes require electron donation from P450 oxidoreductase. The clinical spectrum of P450 oxidoreductase deficiency ranges from severely affected...

Read the complete abstract on PubMed

Topics

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

Share to Adrenal Hyperplasia, Congenital
Share to Bone Diseases, Developmental
Share to Bone Diseases, Metabolic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytochrome P-450 Enzyme System

Share to Genotype

Share to Oxidoreductases

Share to Phenotype

Source

Identifiers

PMID: 16915000
DOI: 10.1097/01.mop.0000236395.71956.5c

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia.PMID 16915000Read ↗

Congenital adrenal hyperplasia and P450 oxidoreductase deficiency.Semantic proximity Read ↗

Cytochrome P450 oxidoreductase deficiency: rare congenital disorder leading to skeletal malformations and steroidogenic defects.Semantic proximity Read ↗

P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia.Semantic proximity Read ↗

Genetics of congenital adrenal hyperplasia.Semantic proximity Read ↗

Diagnostic challenges and management advances in cytochrome P450 oxidoreductase deficiency, a rare form of congenital adrenal hyperplasia, with 46, XX karyotypeSemantic proximity Read ↗

Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study.Semantic proximity Read ↗

A case of Antley-Bixler syndrome caused by compound heterozygous mutations of the cytochrome P450 oxidoreductase gene.Semantic proximity Read ↗

Prenatal diagnosis of congenital adrenal hyperplasia caused by P450 oxidoreductase deficiency.Semantic proximity Read ↗

46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene.Semantic proximity Read ↗

46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical FeaturesSemantic proximity Read ↗

Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiency.Semantic proximity Read ↗

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis.Semantic proximity Read ↗

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