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

Pitfalls in the diagnosis of 5α-reductase type 2 deficiency during early infancy.

Hormone research in paediatrics - 1 Jan 2011

Perry R J, Novikova E, Wallace A M, Donaldson M D C

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to 3-Oxo-5-alpha-Steroid 4-Dehydrogenase
Share to Age Factors
Share to Diagnosis, Differential
Share to Gonadal Dysgenesis, 46,XY

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Neonatal Screening

Share to Pedigree

Source

Identifiers

PMID: 21447938
DOI: 10.1159/000324646

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pitfalls in the diagnosis of 5α-reductase type 2 deficiency during early infancy.PMID 21447938Read ↗

5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian Cohort.Semantic proximity Read ↗

Molecular analysis of 5alpha-reductase type 2 gene in eight unrelated egyptian children with suspected 5alpha-reductase deficiency: prevalence of the G34R mutation.Semantic proximity Read ↗

Failure to Recognize Fetal Alcohol Syndrome in Newborn InfantsSemantic proximity Read ↗

Diagnostic criteria for respiratory chain disorders in adults and children.Semantic proximity Read ↗

The great masquerade: delayed diagnosis of mucopolysaccharidosis in adulthood.Semantic proximity Read ↗

Practitioner review: physical investigations in mental retardation.Semantic proximity Read ↗

Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy.Semantic proximity Read ↗

VLCAD deficiency: pitfalls in newborn screening and confirmation of diagnosis by mutation analysis.Semantic proximity Read ↗

Prenatal diagnosis for alpha1-antitrypsin deficiency.Semantic proximity Read ↗

Retrospective approach to methylenetetrahydrofolate reductase mutations in children.Semantic proximity Read ↗

Homocystinuria patient and caregiver survey: experiences of diagnosis and patient satisfactionSemantic proximity Read ↗

Rapid diagnosis of glucocorticoid suppressible hyperaldosteronism in infants and adolescents.Semantic proximity Read ↗

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