Idiopathic angiokeratoma corporis diffusum [1]

Clinical and Experimental Dermatology

Volumn 22, Issue 4, 1997, Pages 205-207

  Fimiani, M ^a   Mazzatenta, C ^a   Rubegni, P ^a   Andreassi, L ^a  

^a UNIVERSITY OF SIENA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; FABRY DISEASE; HEMANGIOKERATOMA; HUMAN; IDIOPATHIC DISEASE; LETTER; LYSOSOME STORAGE DISEASE; MALE; PAPULE; PRIORITY JOURNAL; SKIN BIOPSY;

EID: 0030807841     PISSN: 03076938     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2230.1997.tb01064.x     Document Type: Letter

References (5)

1. 1 Holmes RC, Fensom AH, McKee P et al. Angiokeratoma corporis diffusum in a with normal enzyme activities. J Am Acad Dermatol 1984 ; 10: 384–7.
2. 2 Crovato F, Rebora A. Angiokeratoma corporis diffusum and normal enzyme activities. J Am Acad Dermatol 1985 ; 5: 885–6.
3. 3 Mardsen J, Allen R. Widespread angiokeratomas without evidence of metabolic disease. Arch Dermatol 1987 ; 123: 1125–7.
4. 4 Calzavara‐Pinton PG, Colombi M, Carlino A et al. Angiokeratoma corporis absence of metabolic disorders. Arch Dermatol 1995 ; 131: 57–62.
5. 5 Eng CM, Desnick RJ. Molecular basis of Fabry disease. Mutations and polymorphisms in the human alpha‐galactosidase A gene. Hum Mutat 1994 ; 3: 103–11.