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

Teebi hypertelorism syndrome: further observations.

American journal of medical genetics - 23 Oct 1995

Tsukahara M, Uchida M, Shinohara T

Abstract excerpt

A new autosomal dominant syndrome resembling craniofrontonasal syndrome was identified by Teebi [1987: Am J Med Genet 28:581-591]. We report on an additional case of Teebi hypertelorism syndrome. A 6-year-old girl presented with brachycephaly, peculiar facial appearance resembling mild frontonasal "dysplasia", small hands and feet with interdigital webbing. In addition, she had previously undescribed...

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 Child
Share to Family

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

Share to Phenotype

Share to Syndrome

Source

Identifiers

PMID: 8849013
DOI: 10.1002/ajmg.1320590113

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

Teebi hypertelorism syndrome: further observations.PMID 8849013Read ↗

Teebi hypertelorism syndrome.Semantic proximity Read ↗

A newly recognized craniosynostosis syndrome with features of Aarskog-Scott and Teebi syndromes.Semantic proximity Read ↗

Frontonasal dysostosis in two successive generations.Semantic proximity Read ↗

New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies.Semantic proximity Read ↗

Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings.Semantic proximity Read ↗

Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies: a third case report.Semantic proximity Read ↗

Cerebro-facio-thoracic dysplasia: expanding the phenotype.Semantic proximity Read ↗

New case of Toriello-Carey syndrome.Semantic proximity Read ↗

Expanding the SPECC1L mutation phenotypic spectrum to include Teebi hypertelorism syndrome.Semantic proximity Read ↗

Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations.Semantic proximity Read ↗

Lethal femoral-facial syndrome: a case with unusual manifestations.Semantic proximity Read ↗

Cerebro-fronto-facial syndrome (Dandy-Walker Variant and frontofacial dysmorphisms): report of the first case identified by increased nuchal translucency beyond 13(+6) weeks.Semantic proximity Read ↗

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