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

Consequences of X-linked hypohidrotic ectodermal dysplasia for the human jaw bone.

Frontiers of oral biology - 1 Jan 2009

Lesot H, Clauss F, Manière M C, Schmittbuhl M

Abstract excerpt

Mutations of the Eda gene, which encodes for ectodysplasin-A1, result in X-linked hypohydrotic ectodermal dysplasia (XLHED). This pathology may lead to severe oligodontia, subsequently requiring implant therapy. Since Eda is suspected to participate in bone development, the jaw bone status was investigated in XLHED patients in order to adjust the surgical protocol. Using computed tomography, densitometric...

Read the complete abstract on PubMed

Topics

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

Share to Anodontia
Share to Bone Density
Share to Bone Remodeling

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ectodermal Dysplasia 1, Anhidrotic

Share to Mandible

Share to Osteogenesis

Share to Radiography

Share to Reference Values

Source

Identifiers

PMID: 19828977
DOI: 10.1159/000242398

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

Consequences of X-linked hypohidrotic ectodermal dysplasia for the human jaw bone.PMID 19828977Read ↗

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 ↗

Anomalies of tooth formation in hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

Anthropometric and cephalometric measurements in X-linked hypohidrotic ectodermal dysplasia.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 ↗

De novo EDA mutations: Variable expression in two Egyptian families.Semantic proximity Read ↗

Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.Semantic proximity Read ↗

Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation.Semantic proximity Read ↗

X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families.Semantic proximity Read ↗

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

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

Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.Semantic proximity Read ↗

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