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2. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity. Oh SW; Kim MY; Lee JS; Kim SC J Dermatol; 2006 Mar; 33(3):161-4. PubMed ID: 16620218 [TBL] [Abstract][Full Text] [Related]
4. A case of pachyonychia congenita with oral leukoplakia and steatocystoma multiplex. Lim TW; Paik JH; Kim NI J Dermatol; 1999 Oct; 26(10):677-81. PubMed ID: 10554435 [TBL] [Abstract][Full Text] [Related]
5. [Pachyonychia congenita with Steatocystoma multiplex: a report of 12 cases in one family [author's transl]]. Aoyagi T; Ohnishi O Nihon Hifuka Gakkai Zasshi; 1976 Sep; 86(11):767-75. PubMed ID: 1034800 [No Abstract] [Full Text] [Related]
7. Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts. Feng YG; Xiao SX; Ren XR; Wang WQ; Liu A; Pan M Br J Dermatol; 2003 Mar; 148(3):452-5. PubMed ID: 12653736 [TBL] [Abstract][Full Text] [Related]
8. Pachyonychia congenita complicated by hidradenitis suppurativa: a family study. Todd P; Garioch J; Rademaker M; Susskind W; Gemell C; Thomson J Br J Dermatol; 1990 Nov; 123(5):663-6. PubMed ID: 2248894 [TBL] [Abstract][Full Text] [Related]
10. Natal teeth and steatocystoma multiplex complicated by hidradenitis suppurativa. A new syndrome. McDonald RM; Reed WB Arch Dermatol; 1976 Aug; 112(8):1132-4. PubMed ID: 988984 [TBL] [Abstract][Full Text] [Related]
11. Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2. Oh Adib C; Jones B; Liao H; Smith FJ; Solomon R; Egan CA; Leachman S Arch Dermatol Res; 2008 Jun; 300(5):211-4. PubMed ID: 18347808 [No Abstract] [Full Text] [Related]
12. Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2. Celebi JT; Tanzi EL; Yao YJ; Michael EJ; Peacocke M J Invest Dermatol; 1999 Nov; 113(5):848-50. PubMed ID: 10571744 [TBL] [Abstract][Full Text] [Related]
13. Pachyonychia congenita with epidermal cysts and teeth at birth: 4th generation. Besser FS Br J Dermatol; 1971 Jan; 84(1):95-6. PubMed ID: 5108274 [No Abstract] [Full Text] [Related]
17. A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a. García-Rio I; Peñas PF; García-Díez A; McLean WH; Smith FJ Br J Dermatol; 2005 Apr; 152(4):800-2. PubMed ID: 15840119 [No Abstract] [Full Text] [Related]
18. Steatocystoma multiplex and oligosymptomatic pachyonychia congenita of the Jackson-Sertoli type. Hohl D Dermatology; 1997; 195(1):86-8. PubMed ID: 9267753 [TBL] [Abstract][Full Text] [Related]
19. Odontoonychodermal dysplasia: a previously apparently undescribed ectodermal dysplasia. Fadhil M; Ghabra TA; Deeb M; Der Kaloustian VM Am J Med Genet; 1983 Feb; 14(2):335-46. PubMed ID: 6837628 [TBL] [Abstract][Full Text] [Related]