Kerinokeratosis papulosa with a type 2 segmental manifestation

Journal of the American Academy of Dermatology

Volumn 50, Issue 5 SUPPL., 2004, Pages 84-85

  Happle, Rudolf ^a   Fleiner, Joachim ^b   Loskamp, Ulrike ^c  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b Laboratory of Dermatohistopathology   (Germany)

^c Loskamp Dermatology Clinic   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARM; ARTICLE; CASE REPORT; FEMALE; GENODERMATOSIS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPERKERATOSIS; KERATOSIS; KERINOKERATOSIS PAPULOSA; PAPULE; PRIORITY JOURNAL; SCHOOL CHILD; SKIN BIOPSY; SKIN DISEASE;

EID: 2342477260     PISSN: 01909622     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0190-9622(03)01489-0     Document Type: Article

References (4)

1. Coleman R, Malone M, Handfield-Jones S, Goodwin P, Rees J, Atherton DJA, et al. Waxy keratoses of childhood. Clin Exp Dermatol 1994;19:173-6.
2. Mehrabi D, Thomas JE, Selim MA, Prose NS. Waxy keratoses of childhood in a segmental distribution. Pediatr Dermatol 2001;18:415-6.
3. Happle R. A rule concerning the segmental manifestation of autosomal dominant skin disorders: review of clinical examples providing evidence for dichotomous types of severity. Arch Dermatol 1997;133:1505-9.
4. Happle R. Segmentale Typ-2-Manifestation autosomal dominanter Hautkrankheiten: Entwicklung eines neuen formalgenetischen Konzeptes. Hautarzt 2001;52:283-7.