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

Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait.

Clinical genetics - 1 May 2003

Tadin-Strapps M, Salas-Alanis J C, Moreno L, Warburton D, Martinez-Mir A, Christiano A M

Abstract excerpt

We report a large Mexican kindred with a variant form of congenital universal hypertrichosis that is inherited in an apparent X-linked recessive manner. In addition to the generalized hypertrichosis, the affected individuals have dental malformations and deafness. Males are more severely affected than females who exhibit only mild hypertrichosis, but not deafness or dental anomalies. Haplotype analysis in this...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Deafness

Share to Genes, Recessive

Share to Genetic Linkage

Share to Hypertrichosis

Share to Mexico

Share to Tooth Abnormalities

Source

Identifiers

PMID: 12752576
DOI: 10.1034/j.1399-0004.2003.00069.x

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

Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X-linked trait.PMID 12752576Read ↗

De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features.Semantic proximity Read ↗

Mapping of the congenital generalized hypertrichosis locus to chromosome Xq24-q27.1.Semantic proximity Read ↗

Dental anomalies in syndromes displaying hypertrichosis in the clinical spectrum.Semantic proximity Read ↗

Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis.Semantic proximity Read ↗

Chromosomal Rearrangements Identified in Three Additional Patients With Generalized Congenital Hypertrichosis With Gingival Hyperplasia Involving the 17q24.2-q24.3 Locus.Semantic proximity Read ↗

Congenital hypertrichosis universalis in Mexican female twins.Semantic proximity Read ↗

[Tooth and oral mucosa hereditary anomalies in complex syndromes characterized by hyper- or hypotrichosis].Semantic proximity Read ↗

Phenotypic findings in Chinese families with X-linked hypohydrotic ectodermal dysplasia.Semantic proximity Read ↗

X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.Semantic proximity Read ↗

Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions.Semantic proximity Read ↗

Strong association of the SNP rs17822931 with wet earwax and bromhidrosis in a Chinese family.Semantic proximity Read ↗

A novel X-linked dominant condition: X-linked congenital isolated ptosis.Semantic proximity Read ↗

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