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

Anomalies of tooth formation in hypohidrotic ectodermal dysplasia.

International journal of paediatric dentistry - 1 Jan 2007

Lexner Michala O, Bardow Allan, Hertz Jens Michael, Nielsen Lis A, Kreiborg Sven

Abstract excerpt

OBJECTIVE: The X-linked hypohidrotic ectodermal dysplasia (HED) is the most common type of ectodermal dysplasia. The clinical identification of possible heterozygous females can be difficult because of the varying degrees of clinical signs caused by X-chromosome inactivation. This study is the fi...

Read the complete abstract on PubMed

Topics

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

Share to Anodontia
Share to Biomarkers
Share to Ectodermal Dysplasia 1, Anhidrotic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heterozygote

Share to Incisor

Share to Tooth Abnormalities

Share to Tooth Root

Source

Identifiers

PMID: 17181574
DOI: 10.1111/j.1365-263X.2006.00801.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17181574-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Anomalies of tooth formation in hypohidrotic ectodermal dysplasia.PMID 17181574Read ↗

Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review.Semantic proximity Read ↗

X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.Semantic proximity Read ↗

Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesisSemantic proximity Read ↗

From ectodermal dysplasia to selective tooth agenesis.Semantic proximity Read ↗

The genetic basis of hypodontia in dental development.Semantic proximity Read ↗

Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.Semantic proximity Read ↗

Multistage orthodontic-implantology-prosthetic treatment of a patient diagnosed with hypohidrosis ectodermal dysplasia syndrome with EDAR mutation: a case report.Semantic proximity Read ↗

EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature.Semantic proximity Read ↗

Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated Genes.Semantic proximity Read ↗

[Detection of EDA gene mutation and phenotypic analysis in patients with hypohidrotic ectodermal dysplasia].Semantic proximity Read ↗

X-linked hypohidrotic ectodermal dysplasia. Genetic and dental findings in 67 Danish patients from 19 families.Semantic proximity Read ↗

Genetics and human malformations.Semantic proximity Read ↗

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