What is poikiloderma?

Dermatology

Volumn 207, Issue 3, 2003, Pages 243-245

  Lipsker, Dan ^a  

^a UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DYSKERATOSIS CONGENITA; EDITORIAL; HUMAN; HYPERPIGMENTATION; PHOTOSENSITIVITY DISORDER; POIKILODERMA; PRIORITY JOURNAL; RADIATION DERMATITIS; SKIN ATROPHY; SKIN DISCOLORATION; SKIN DISEASE; TELANGIECTASIA;

ADOLESCENT; ADULT; AGE FACTORS; BIOPSY, NEEDLE; CHILD; CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; LUPUS ERYTHEMATOSUS, CUTANEOUS; MALE; PROGNOSIS; RISK ASSESSMENT; ROTHMUND-THOMSON SYNDROME;

EID: 0142227882     PISSN: 10188665     EISSN: None     Source Type: Journal    
DOI: 10.1159/000073082     Document Type: Editorial

References (16)

1. Marzano AV, Facchietti M, Alessi E. Poikilodermatous subacute cutaneous lupus erythematosus. Dermatology 2003;207:285-291.
2. Itin PH, Lautenschlager S: Genodermatosis with reticulate, patchy and mottled pigmentation of the neck - A clue to rare dermatologic disorders. Dermatology 1998;197:281-290.
3. Itin PH, Lautenschlager S: Reticulate, patchy and mottled pigmentation of the neck: Acquired forms. Dermatology 1998;197:291-296.
4. Weedon D: Skin Pathology. Edinburgh, Churchill Livingstone, 1997.
5. Marghescu S: Réflexions sur la classification des poïkilodermies congénitales. Ann Dermatol Véné réol 1987;114:255-259.
6. Kavanagh GM, Jardine PE, Peachey RD, Murray JC, De Becker D: The scleroatrophic syndrome of Huriez. Br J Dermatol 1997;137:114-118.
7. Antinolo G, Nieto M, Borrego S, Sierra J, Rufo M, Siljestrom ML: Familial spastic paraplegia with neuropathy and poikiloderma: A new syndrome? Clin Genet 1992;41:281-284.
8. Balraj P, Concannon P, Jamal R, Beghini A, Hoe TS, Khoo AS, Volpi L: An unusual mutation in RECQ4 gene leading to Rothmund-Thomson syndrome. Mutat Res 2002;508:99-105.
9. Wang LL, Levy ML, Lewis RA, Chintagumpala MM, Lev D, Rogers M, Plon SE: Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients. Am J Med Genet 2001;102:11-17.
10. Vulliamy T, Marrone A, Goldman F, Dearlove A, Bessler M, Mason PJ, Dokal I: The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature 2001;413:432-435.
11. Krunic AL, Ljiljana M, Novak A, Carlos G, Clark RE: Hereditary bullous acrokeratotic poikiloderma of Weary-Kindler associated with pseudoainhum and sclerotic bands. Int J Dermatol 1997;36:529-533.
12. Binder B, Metze D, Smolle J: Kongenitale bullop̈se Poikilodermie (Kindler-Syndrom). Hautarzt 2002;53:546-549.
13. Weary PE, Hsu YT, Richardson DR, Caravati CM, Wood BT: Hereditary sclerosing poikiloderma: Report of two families with an unusual and distinctive genodermatosis. Arch Dermatol 1969;100:413-422.
14. Verloes A, Soyeur-Broux M, Arrese-Estrada J, Piérard-Franchimont C, Dodinval P, Piérard GE: Poikiloderma, alopecia, retrognathism and cleft palate: The PARC syndrome. Is this an undescribed dominantly inherited syndrome? Dermatologica 1990;181:142-144.
15. Fierens F, Bourlond A, Clerens A, Guilmot-Bruneau MM, Defresne C: Etat poïkilodermique et tolamolol. Dermatologica 1982;164:109-114.
16. 12. J Clin Pathol 1994;47:956-958.