A case of pachyonychia congenita with oral leukoplakia and steatocystoma multiplex

Journal of Dermatology

Volumn 26, Issue 10, 1999, Pages 677-681

  Lim, Tuk Woo ^a   Paik, Jong Hyun ^a   Kim, Nack In ^a  

^a Kyung Hee University Hospital   (South Korea)

Author keywords

Pachyonychia congenita; Steatocystoma multiplex

Indexed keywords

RETINOIC ACID;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CONGENITAL PACHYONYCHIA; GENODERMATOSIS; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; LEUKOPLAKIA; MALE; NAIL COLOR DEFECT; NAIL DYSTROPHY; ORAL DRUG ADMINISTRATION; SEBACEOUS CYST;

EID: 0032711772     PISSN: 03852407     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1346-8138.1999.tb02071.x     Document Type: Article

References (18)

1. Schönfeld PHIR: The pachyonychia congenita syndrome, Acta Dermatol Venereol (Stockh), 60: 45-49, 1980.
2. Hodes ME, Norins AL: Pachyonychia congenita and steatocystoma multiplex, Clin Genet, 9: 273-278, 1995
3. Harber RM, Rose TH: Autosomal recessive pachyonychia congenita, Arch Dermatol, 122: 919-923, 1986
4. Chong Hai T, Rajagopalan DDM: Pachyonychia congenita with recessive inheritance, Arch Dermatol, 113: 685-686, 1977.
5. Jadassohn J, Lewandowsky F: Pachyonychia congenita, in Neisser A, Jacobi E, (eds): Ikonographia Dermatologica Urban & Schwarzenberg, Baltimore, Md, 1906, p29-31 (cited from ref. No. 12).
6. Steiglitz JB, Centerwall WR: Pachyonychia congenita (Jadassohn-Lewandowsky syndrome): A 17 member, 4-generation pedigree with unusual respiratory and dental involvement. Am J Med Genet, 14: 21-28, 1983.
7. Forslind B, Nylen B, Swanbeck G, Thyresson M, Thyresson N: Pachyonychia congenita. A histologic and microradiographic study, Acta Dermatol Venereol (Stockholm), 53: 211-216, 1973.
8. Su WPD, Chun SI, Haminand DE, Gordon H: Pachyonychia congenita: A clinical study of 12 cases and review of the literature, Pediatr Dermatol, 7: 33-38, 1990.
9. Chang A, Lucker GPH, Van de Kerkhof PCM, Steijlen PM: Pachyonychia congenita in the absence of other syndrome abnormalities, J Am Acad Dermatol, 19: 521-522, 1994.
10. Pryce DW, Verbov JL: A family with pachyonychia congenita affecting the nails only, Clin Exp Dermatol, 19: 521-522, 1994.
11. Rook A Dawber R: Hereditary and congenital alopecia and hypotrichosis, in Rook A, Dawber R (eds): Disease of the Hair and Scalp, Blackwell Scientific Publications, Oxfold, 1982, p 175.
12. Stephen F, Stewart E: Pachyonychia congenita-associated alopecia: A microscopic analysis using transverse section technique, Am J Dermatopathol, 19: 180-184, 1997.
13. Kim JU, Nogita T, Terajima S, et al: Pachyonychia congenita associated with steatocystoma multiplex, J Dermatol, 25: 479-481, 1998.
14. Smith FJ, Jonkman MF, van Goor H, et al: A mutation in human keratin K6b produces a phenotype of the K17 disorder pachyonychia congenita type 2, Hum Mol Genet, 7: 1143-1148, 1998.
15. McLean WH, Rugg EL, Lunny DP, et al: Keratin 16 and keratin 17 mutation cause pachyonychia congenita. Nature Genet, 9: 273-278, 1995.
16. Munro CS, Carter S, Bryce S, et al: A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21, J Med Genet, 31: 675-678, 1994.
17. Bowden PE, Haley JL, Kansky A, et al: Mutation of a type II keratin gene (K6a) in pachyonychia congenita, Nature Genet, 10: 363-365, 1995.
18. Thomas DR, Jorizzo JL, Brysk MM, et al: Pachyonychia congenita, Arch Dermatol, 120: 1475-1479, 1984.