Literature DB >> 11310247

Dyskeratosis congenita: report of a case.

C J Brown1.   

Abstract

Dyskeratosis congenita is a rare multisystem condition involving mainly the ectoderm. It is characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. Oral and dental abnormalities may also be present. Complications are a predisposition to malignancy and bone marrow involvement with pancytopenia. The case of a 14-year-old girl is described who presented with several of the characteristic systemic features of this condition, together with the following oral features: hypodontia, diminutive maxillary lateral incisors, delayed dental eruption, crowding in the maxillary premolar region, short roots, poor oral hygiene, gingival inflammation and bleeding, alveolar bone loss, caries and a smooth atrophic tongue with leukoplakia. Although this condition is rare, dental surgeons should be aware of the dental abnormalities that exist and the risk of malignant transformation within the areas of leukoplakia.

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Year:  2000        PMID: 11310247     DOI: 10.1046/j.1365-263x.2000.00214.x

Source DB:  PubMed          Journal:  Int J Paediatr Dent        ISSN: 0960-7439            Impact factor:   3.455


  2 in total

1.  Oral and dental phenotype of dyskeratosis congenita.

Authors:  J C Atkinson; K E Harvey; D L Domingo; M I Trujillo; J P Guadagnini; S Gollins; N Giri; T C Hart; B P Alter
Journal:  Oral Dis       Date:  2008-07       Impact factor: 3.511

2.  Oral and dental findings of dyskeratosis congenita.

Authors:  Mine Koruyucu; Pelin Barlak; Figen Seymen
Journal:  Case Rep Dent       Date:  2014-12-24
  2 in total

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