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

Twenty-four cases of the EEC syndrome: clinical presentation and management.

Journal of medical genetics - 1 Sept 1995

Buss P W, Hughes H E, Clarke A

Abstract excerpt

Twenty-four cases of EEC syndrome were identified as part of a nationwide study. Ectodermal dysplasia, by study definition, was present in all cases and hair and teeth were universally affected. Nail dysplasia was present in 19 subjects (79%) and the skin was affected in 21 (87%). The presence of hypohidrosis was not noted as a predominant feature in the syndrome and its occurrence appeared to depend on the...

Read the complete abstract on PubMed

Topics

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

Share to Abnormalities, Multiple
Share to Adolescent
Share to Child

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

Share to Child, Preschool

Share to Genetic Linkage

Share to Infant

Share to Pedigree

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 8544192
DOI: 10.1136/jmg.32.9.716
PMCID: PMC1051673

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Twenty-four cases of the EEC syndrome: clinical presentation and management.PMID 8544192Read ↗

Ectodermal dysplasias: a new clinical-genetic classification.Semantic proximity Read ↗

Ectodermal Dysplasia: A Genetic ReviewSemantic proximity Read ↗

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathwaySemantic proximity Read ↗

Ocular and non-ocular manifestations of hypohidrotic ectodermal dysplasia.Semantic proximity Read ↗

A classical variant of ectodermal dysplasia: a case report.Semantic proximity Read ↗

EEC syndrome: Report on 20 new patients, clinical and genetic considerationsSemantic proximity Read ↗

A newborn with overlapping features of AEC and EEC syndromes.Semantic proximity Read ↗

Towards a unified classification of the ectodermal dysplasias: opportunities outweigh challenges.Semantic proximity Read ↗

Prevalence and Patient Characteristics of Ectodermal Dysplasias in DenmarkSemantic proximity Read ↗

Hypohidrotic Ectodermal Dysplasias: Phenotypic and Genotypic Findings in 32 Cases.Semantic proximity Read ↗

Ectodermal dysplasias: an overview and update of clinical and molecular-functional mechanisms.Semantic proximity Read ↗

Oligodontia in the Clinical Spectrum of Syndromes: A Systematic ReviewSemantic proximity Read ↗

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