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Article

[Dental alterations in junctional epidermolysis bullosa--report of a patient with a mutation in the LAMB3-gene].

Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG - 1 May 2005

Sadler Elke, Laimer Martin, Diem Anja, Klausegger Alfred, Pohla-Gubo Gabriele, Muss Wolfgang, Hachleitner Johannes, Stadlhuber Rudolf, Bauer Johann W, Hintner Helmut

Abstract excerpt

During early odontogenesis the basement membrane is known to be important in epithelio-mesenchymal interactions. Mutations in the gene of one of the major structural proteins of the basement membrane such as laminin 5 might therefore be expected either to seriously compromise ameloblast differentiation and/ or interfere with normal basement-membrane formation and degradation and thus the binding of the...

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Source

Identifiers

PMID: 16372803
DOI: 10.1111/j.1610-0387.2005.05703.x

Genes

LAMB3

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

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Research trail→

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[Dental alterations in junctional epidermolysis bullosa--report of a patient with a mutation in the LAMB3-gene].PMID 16372803Read ↗

LAMB3 Mutations Causing Autosomal-dominant Amelogenesis ImperfectaSemantic proximity Read ↗

Do mutations in the basement membrane zone affect the human periodontium? Review with special reference to epidermolysis bullosa.Semantic proximity Read ↗

[Hereditary epidermolysis bullosa: towards classification and genetic counseling based upon identification of molecular defects].Semantic proximity Read ↗

Oral manifestations of epidermolysis bullosa dystrophica: a rare genetic disease.Semantic proximity Read ↗

Inherited epidermolysis bullosa: an update and suggested dental care considerations.Semantic proximity Read ↗

Enamel defects in carriers of a novel LAMA3 mutation underlying epidermolysis bullosa.Semantic proximity Read ↗

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

An intronic variant in LAMB3 contributes to junctional epidermolysis bullosa and enamel hypoplasia via translational attenuation.Semantic proximity Read ↗

Molecular basis of non-lethal junctional epidermolysis bullosa: identification of a 38 basepair insertion and a splice site mutation in exon 14 of the LAMB3 gene.Semantic proximity Read ↗

[Phenotype analysis and the molecular mechanism of enamel hypoplasia].Semantic proximity Read ↗

[Genetic, clinical and molecular analysis of a family affected by amelogenesis imperfecta].Semantic proximity Read ↗

Compound heterozygosity for an out-of-frame deletion and a splice site mutation in the LAMB3 gene causes nonlethal junctional epidermolysis bullosa.Semantic proximity Read ↗

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