Useful applications of DNA repair tests for differential diagnosis of atypical dyschromatosis symmetrica hereditaria from xeroderma pigmentosum

British Journal of Dermatology

Volumn 144, Issue 1, 2001, Pages 162-168

  Ohtoshi, E ^a   Matsumura, Y ^a   Nishigori, C ^a   Toda, K I ^a   Horiguchi, Y ^b   Ikenaga, M ^a   Miyachi, Y ^a  

^a KYOTO UNIVERSITY   (Japan)

^b OSAKA RED CROSS HOSPITAL   (Japan)

Author keywords

Dyschromatosis symmetrica hereditaria; Ultraviolet light; Unscheduled DNA synthesis; Xeroderma pigmentosum

Indexed keywords

AGED; ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; COLONY FORMATION; DEPIGMENTATION; DIAGNOSTIC ACCURACY; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DNA REPAIR; DNA SYNTHESIS; DYSCHROMATOSIS SYMMETRICA HEREDITARIA; FEMALE; GENETIC DISORDER; HUMAN; HUMAN TISSUE; LENTIGO; MALE; PHOTOSENSITIVITY; PRIORITY JOURNAL; SKIN DISEASE; SKIN FIBROBLAST; SKIN PIGMENTATION; SUNBURN; ULTRAVIOLET RADIATION; XERODERMA PIGMENTOSUM;

AGED; CELL CULTURE TECHNIQUES; CELL SURVIVAL; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; DNA REPAIR; FIBROBLASTS; HUMANS; MALE; PIGMENTATION DISORDERS; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM;

EID: 0035128714     PISSN: 00070963     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2133.2001.03968.x     Document Type: Article

References (33)

1. Dyschromatosis symmetrica hereditaria
2. Symmetrische Pigmentanomalie der Extremitaten
3. Statistical study of dyschromatosis symmetrica hereditaria
4. Pigmentary disorders
5. Eine besondere form der akropigmentation: Acropigmentatio reticularis
6. Reticulate acropigmentation of Kitamura
7. Reticulate pigmentary disorder - A review
8. Clinical and photobiological differences between dyschromatosis symmetrica hereditaria and xeroderma pigmentosum
9. A case of xeroderma pigmentosum with clinical appearance of dyschromatosis symmetrica hereditaria
10. Somatic mosaicism for DNA repair capacity in fibroblasts derived from a group A xeroderma pigmentosum patient
11. Recovery from ultraviolet light-induced depression of ribosomal RNA synthesis in normal human, xeroderma pigmentosum and Cockayne syndrome cells
12. Sensitivity to UV radiation of fibroblasts from a Japanese group A xeroderma pigmentosum patient with mild neurological abnormalities
13. Assignment of three Chinese xeroderma pigmentosum patients to complementation group C and one to group E
14. Dyschromatosis
15. Disorders of melanocytes
16. Spectrum of reticulate flexural and acral pigmentary disorder in northern India
17. Overlap of reticulate acropigmentation of Kitamura, acropigmentation of Dohi and Dowling-Degos disease in four generations
18. Acropigmentation of Dohi in a 12-year-old boy
19. Dyschromatosis symmetrica hereditaria in an Indian family
20. Dyschromatosis symmetrica hereditaria - A histochemical and ultrastructual study
21. Dyschromatosis symmetrica hereditaria affecting two families
22. Neurofibromatosis and reticulate acropigmentation of Dohi: A case report
23. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report
24. Familial reticulate acropigmentation of Dohi
25. Reticulate acropigmentation of Dohi
26. Disorders of skin colour
27. Dyschromatosis
28. Disorders of brown macules
29. Dyschromatosis
30. Dyschromatosis symmetrica hereditaria
31. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): Report of a Japanese family with the condition and a literature review of 185 cases
32. Density of dopa-positive melanocytes in dyschromatosis symmetrica hereditaria
33. A case of systemic sclerosis with dyschromatosis symmetrica hereditaria with unusual clinical appearances