Literature DB >> 23257645

Management of a xeroderma pigmentosum case with oral findings in a dental setup.

Vanaja Reddy Banda1, Naveen Reddy Banda, Ramesh Reddy, Praveen Banda.   

Abstract

Xeroderma pigmentosum (XP) is heterogeneous group of disorder transmitted as autosomal recessive trait. It is characterised by photosensitivity, freckled pigmentation and premature skin ageing and malignant tumour development. The manifestations are due to a cellular hypersensitivity to ultraviolet light resulting from a defect in DNA repair. Multiple cutaneous neoplasms develop at a young age in persons with XP. Two important causes of mortality are metastatic malignant melanoma and squamous cell carcinoma (SCC). We report a case of XP in a 22 year-old male patient who developed SCC of lower lip with in a short period of 1 month.

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Year:  2012        PMID: 23257645      PMCID: PMC4543547          DOI: 10.1136/bcr-2012-007521

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  3 in total

1.  Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels.

Authors:  F Chavanne; B C Broughton; D Pietra; T Nardo; A Browitt; A R Lehmann; M Stefanini
Journal:  Cancer Res       Date:  2000-04-01       Impact factor: 12.701

Review 2.  Xeroderma pigmentosum.

Authors:  Johannes Norgauer; Marco Idzko; Elisabeth Panther; Oliver Hellstern; Yared Herouy
Journal:  Eur J Dermatol       Date:  2003 Jan-Feb       Impact factor: 3.328

3.  Xeroderma pigmentosum: a case report.

Authors:  Sam Park; Murray Dock
Journal:  Pediatr Dent       Date:  2003 Jul-Aug       Impact factor: 1.874

  3 in total
  1 in total

Review 1.  Xeroderma pigmentosum: an updated review.

Authors:  Alexander Kc Leung; Benjamin Barankin; Joseph M Lam; Kin Fon Leong; Kam Lun Hon
Journal:  Drugs Context       Date:  2022-04-25
  1 in total

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