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Article

Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.

Journal of medical genetics - 1 Feb 2000

Hart T C, Hart P S, Michalec M D, Zhang Y, Marazita M L, Cooper M, Yassin O M, Nusier M, Walker S

Abstract excerpt

Prepubertal periodontitis (PPP) is a rare and rapidly progressive disease of young children that results in destruction of the periodontal support of the primary dentition. The condition may occur as part of a recognised syndrome or may occur as an isolated finding. Both autosomal dominant and recessive forms of Mendelian transmission have been reported for PPP. We report a consanguineous Jordanian family with...

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Identifiers

PMID: 10662808
DOI: 10.1136/jmg.37.2.95
PMCID: PMC1734516

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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.

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Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.PMID 10662808Read ↗

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