Duś M, Gornowicz J, Dmochowski M. Case reportTransient manifestation of dermatitis herpetiformis in a female with familial predisposition induced by propafenone. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii. 2009;26(4):239-242.
APA
Duś, M., Gornowicz, J., & Dmochowski, M. (2009). Case reportTransient manifestation of dermatitis herpetiformis in a female with familial predisposition induced by propafenone. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, 26(4), 239-242.
Chicago
Duś, Monika, Justyna Gornowicz, and Marian Dmochowski. 2009. "Case reportTransient manifestation of dermatitis herpetiformis in a female with familial predisposition induced by propafenone". Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii 26 (4): 239-242.
Harvard
Duś, M., Gornowicz, J., and Dmochowski, M. (2009). Case reportTransient manifestation of dermatitis herpetiformis in a female with familial predisposition induced by propafenone. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, 26(4), pp.239-242.
MLA
Duś, Monika et al. "Case reportTransient manifestation of dermatitis herpetiformis in a female with familial predisposition induced by propafenone." Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii, vol. 26, no. 4, 2009, pp. 239-242.
Vancouver
Duś M, Gornowicz J, Dmochowski M. Case reportTransient manifestation of dermatitis herpetiformis in a female with familial predisposition induced by propafenone. Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii. 2009;26(4):239-242.
Dermatitis herpetiformis (DH) is an autoimmune blistering disorder pathogenetically associated with a gluten-dependent enteropathy. It is characterized by intensively pruritic, symmetrically distributed papulovesicular lesions found mainly on the extensor surfaces of the forearms, elbows, knees and gluteal region. Familial occurrence is frequently observed. Many drugs and chemical substances are triggers of the disease. In the paper the case of a 29-year-old woman with DH induced by propafenone and a positive familial history of DH is described.
