Familial coincidence of hidradenitis suppurativa and steatocystoma multiplex: Viewpoints in dermatology • Correspondence

Clinical and Experimental Dermatology

Volumn 35, Issue 4, 2010, Pages

  Hollmig, T ^a   Menter, A ^b  

^a SOUTHWESTERN UNIVERSITY   (United States)

^b BAYLOR UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSCESS; ACNE CONGLOBATA; ADULT; CASE REPORT; CELLULITIS; FEMALE; HUMAN; LETTER; MALE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SEBACEOUS CYST; SKIN BIOPSY; SKIN NODULE; SUPPURATIVE HIDRADENITIS;

ADULT; CHILD, PRESCHOOL; FEMALE; HIDRADENITIS SUPPURATIVA; HUMANS; MALE; PACHYONYCHIA CONGENITA; PEDIGREE; SKIN DISEASES, GENETIC;

EID: 77951211126     PISSN: 03076938     EISSN: 13652230     Source Type: Journal    
DOI: 10.1111/j.1365-2230.2009.03742.x     Document Type: Letter

References (4)

1. McDonald RM, Reed WB. Natal teeth and steatocystoma multiplex complicated by hidradenitis suppurativa. Arch Dermatol 1976 112 : 1132 1134.
2. Loo WJ, Rytina E, Todd PM. Hidradenitis suppurativa, Dowling-Degos and multiple epidermal cysts: a new follicular occlusion triad. Clin Exp Dermatol 2004 29 : 622 624. (Pubitemid 39573651)
3. Todd P, Garioch J, Rademaker M et al. Pachyonychia congenita complicated by hidradenitits suppurativa: a family study. Br J Dermatol 1990 123 : 636 666. (Pubitemid 20377659)
4. Covello SP, Smith FJD, Sillevis Smitt JH et al. Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2. Br J Dermatol 1998 139 : 475 480.