Pachyonychia congenita associated with steatocystoma multiplex

Journal of Dermatology

Volumn 25, Issue 7, 1998, Pages 479-481

  Kim, Joong Uhk ^a   Nogita, Toshitatsu ^a   Terajima, Satomi ^a   Kawashima, Makoto ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

Pachyonychia congenita; Steatocystoma multiplex

Indexed keywords

ADULT; ARTICLE; CASE REPORT; GENE MUTATION; HISTOLOGY; HUMAN; MALE; MISSENSE MUTATION; NAIL DISEASE; PARONYCHIA; SEBACEOUS CYST; SKIN DISCOLORATION; SKIN NODULE; SKIN TUMOR;

EID: 0031851581     PISSN: 03852407     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1346-8138.1998.tb02439.x     Document Type: Article

References (8)

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2. Wilson AG: Three cases of hereditary hyperkeratosis of the nail-bed, Br J Dermatol, 17: 13-14, 1905.
3. Jadassohn J, Lewandowsky F: Pachyonychia congenita. Keratosis disseminata circumscripta (follicularis), Tyomata. Leukokeratosis linguae, vol 1, in: Jacobs Ikonographia Dermatologica, Urban and Schwarzenberg, Berlin, 1906, pp 29-31.
4. Akesson HO: Pachyonychia congenita in six generations, Hereditas, 58: 103-110, 1967.
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7. Smith FJD, Corden LD, Rugg EL, et al: Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex, J Invest Dermatol, 108: 220-223, 1997.
8. Jackson ADM, Lawler SD: Pachyonychia congenita: A report of six cases in one family, Ann Eugen, 16: 142-146, 1951.