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Cockayne's syndrome: a case report. Literature review.

Medicina oral, patologia oral y cirugia bucal - 1 May 2006

Arenas-Sordo María de la Luz, Hernández-Zamora Edgar, Montoya-Pérez Luis Alberto, Aldape-Barrios Beatriz Catalina

Abstract excerpt

Cockayne s syndrome is a genetic disorder with a recessive autosomal inheritance, described first by Cockayne in 1936. Patients with this syndrome present failure to thrive, short stature, premature aging, neurological alterations, photosensitivity, delayed eruption of the primary teeth, congenitally absent of some permanent teeth, partial macrodontia, atrophy of the alveolar process and caries. It could be...

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Identifiers

PMID: 16648759

Genes

ERCC6
ERCC8

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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.

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