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Article

Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG - 1 Feb 2010

Mayer Dagmara E Y, Baal Christian, Litschauer-Poursadrollah Margaritha, Hemmer Wolfgang, Jarisch Reinhart

Abstract excerpt

The tricho-dento-osseous syndrome is a rare genetic disorder due to a mutation in the DLX3 gene on chromosome 17q21. It can affect hair, teeth, bone and nails, causing phenotypic variability. We report on an 8-year-old girl with tricho-dento-osseous syndrome, who presented in our allergy center w...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20151948
DOI: 10.1111/j.1610-0387.2009.07125_supp.x

Genes

DLX3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20151948-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.PMID 20151948Read ↗

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

DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes.Semantic proximity Read ↗

Identification of a mutation in DLX3 associated with tricho-dento- osseous (TDO) syndromeSemantic proximity Read ↗

A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation.Semantic proximity Read ↗

Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity.Semantic proximity Read ↗

Craniofacial variations in the tricho-dento-osseous syndrome.Semantic proximity Read ↗

Differential Effects of DLX3 Mutations Drive Phenotypic Variability in Tricho-Dento-Osseous Syndrome via Direct Activation of WNT10A.Semantic proximity Read ↗

Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome.Semantic proximity Read ↗

DLX3 mutation in a new family and its phenotypic variations.Semantic proximity Read ↗

Analysis of the tricho-dento-osseous syndrome genotype and phenotype.Semantic proximity Read ↗

DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome.Semantic proximity Read ↗

DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontism.Semantic proximity Read ↗

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