Results 11 to 20 of about 281 (139)
Acrokeratosis verruciformis of HOPF associated with dilated cardiomyopathy
Indian Journal of Dermatology, 2009 Kaliyadan Feroze +2 more
doaj +4 more sources
Multiple Yellowish and Keratotic Papules in the Thenar Eminence [PDF]
Revista da Sociedade Portuguesa de Dermatologia e Venereologia, 2020 .
Joana Calvão +3 more
doaj +3 more sources
“Clinical Overlap of Darier's Disease and Acrokeratosis Verruciformis of Hopf”: A Case Report [PDF]
Clinical Case ReportsDarier's disease and Acrokeratosis Verruciformis of Hopf can exhibit overlapping clinical features due to mutations in the same ATP2A2 gene. Recognizing this genetic and phenotypic overlap is crucial for accurate diagnosis, genetic counseling, and ...
Mahesh Mathur +5 more
doaj +2 more sources
Acrokeratosis verruciformis of Hopf: A rare presentation in a young Indian female—A case report and review [PDF]
Journal of Family Medicine and Primary CareAcrokeratosis verruciformis of Hopf (AVH) is a rare dermatological disorder associated with keratotic lesions primarily on the dorsal surfaces of the hands and feet, caused by a missense mutation in the ATP2A2 gene.
Gyanendra Singh +3 more
doaj +2 more sources
Acrokeratosis verruciformis of Hopf in an immunosuppressed adult: an exclusive occurrence
Journal of the Egyptian Women’s Dermatologic Society, 2021 Acrokeratosis verruciformis of Hopf (AKV) is a rare autosomal dominant genodermatosis. It can be characterized by warty papules with a symmetrical distribution involving dorsae of hands and feet. It can also involve elbows, knees, nails, and palms. It is
Guneet Awal +2 more
doaj +2 more sources
Macular variant of acrokeratosis verruciformis of Hopf
Medical Journal of Dr. D.Y. Patil University, 2017 Acrokeratosis verruciformis (AKV) of Hopf is an autosomal dominant condition characterized by multiple flesh-colored or lightly pigmented flat or convex warty papules over dorsa of hands, feet, knees, elbows, and forearms.
Rita Vipul Vora +4 more
doaj +2 more sources
Acrokeratosis Verruciformis of Hopf
Archives of Dermatology, 1972 A 67-year-old white man had typical signs of acrokeratosis verruciformis of Hopf. Unusual aspects of the case were late onset of the lesions and lack of a family history of the condition. Observations by past authors are reviewed, and possible linkage with Darier's disease is discussed.
William A. Schueller
openaire +3 more sources
Acitretin treatment in acrokeratosis verruciformis of Hopf
Journal of Dermatological Treatment, 2007 Acrokeratosis verruciformis of Hopf is a rare disorder and characterized by flesh-coloured, wart-like, flat papules on the dorsum of the hands and feet. The disease is an autosomal disorder, but sporadic cases also occur. We present a 38-year-old woman diagnosed with acrokeratosis verruciformis without family history and treated successfully with ...
Serarslan, Gamze +2 more
openaire +3 more sources
Acrokeratosis Verruciformis of Hopf (Hopf Disease)
Journal of Infectious Diseases and Therapy, 2014 Acrokeratosis verruciformis of Hopf is an autosomal dominant genodermatosis usually presenting with multiple planar wart-like lesions, typically observed on the dorsum of the hands, feet, elbows, and knees. The disease is very rare and the pathogenesis remains unknown.
Hussein Salman Waiel Osman
openaire +2 more sources