A distinct type of palmoplantar keratoderma

Pediatric Dermatology

Volumn 26, Issue 1, 2009, Pages 113-115

  Mohammad Ali, Mapar ^a,b   Azarbaik, M ^c  

^a AHVAZ JUNDISHAPUR UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b AHVAZ JUNDISHAPUR UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CORNEA; EXTERNAL EAR; HUMAN; HYPERKERATOSIS; LABORATORY TEST; LIP; MALE; PALMOPLANTAR KERATODERMA; PRESCHOOL CHILD; PRIORITY JOURNAL; SKIN DEFECT; SLIT LAMP;

CHILD; CORNEA; EAR; FOOT DERMATOSES; HAND DERMATOSES; HUMANS; KERATODERMA, PALMOPLANTAR; LIP; MALE; MOUTH; SKIN;

EID: 60449090173     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/j.1525-1470.2008.00845.x     Document Type: Article

References (3)

1. Camisa C, Rossna C. Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Arch Dermatol 1984 120 : 1323 1328.
2. Heimer WL, Brauner G, James WD. Dermatopathia pigmentosa reticularis: a report of a family demonstrating autosomal dominant inheitance. J Am Acad Dermatol 1992 26 : 298 301.
3. Bu TS, Kim YK, Whang KU. A case of dermatopathia pigmentosa reticularis. J Dermatol 1997 24 : 266 269.