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

Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity.

Clinical and experimental dermatology - 1 Sept 2004

Yan K L, He P P, Yang S, Li M, Yang Q, Ren Y Q, Cui Y, Gao M, Xiao F L, Huang W, Zhang X J

Abstract excerpt

Marie Unna hereditary hypotrichosis (MUHH) is a rare autosomal dominant disorder with progressive hair loss starting in early childhood and aggravating at puberty. Several studies have mapped the MUHH gene to chromosome 8p21. Here we report a Chinese MUHH family with variable phenotypes. All affected individuals have anomalies affecting both hair density and hair shafts. Major clinical characteristics, disease...

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Genetic Linkage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Hypotrichosis

Share to Pedigree

Source

Identifiers

PMID: 15347323
DOI: 10.1111/j.1365-2230.2004.01570.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

Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity.PMID 15347323Read ↗

Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.Semantic proximity Read ↗

Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.Semantic proximity Read ↗

Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosis.Semantic proximity Read ↗

Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation.Semantic proximity Read ↗

Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.Semantic proximity Read ↗

Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.Semantic proximity Read ↗

Update of recent findings in genetic hair disorders.Semantic proximity Read ↗

Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood.Semantic proximity Read ↗

Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies.Semantic proximity Read ↗

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.Semantic proximity Read ↗

Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias.Semantic proximity Read ↗

A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities.Semantic proximity Read ↗

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