Results 21 to 30 of about 281 (139)
Acrokeratosis Verruciformis of Hopf: A Rare Case Report [PDF]
Journal of Krishna Institute of Medical Sciences University, 2015 Acrokeratosis Verruciformis of Hopf (AKV) is rare autosomal dominant cutaneous dermatosis described by Hopf in 1931. It is presented at birth but may appear in early child hood; sometimes the onset may be delayed until fifth decade of life.
R. M. Potekar +4 more
doaj +1 more source
Seborrheic keratosis in an adolescent: A rare presentation. [PDF]
Clin Case Rep, 2023 Key Clinical Message Seborrheic keratosis is a common benign epidermal lesion that typically occurs in the elderly population. Its occurrence in childhood and adolescence is rare and can pose a diagnostic challenge for clinicians and dermatopathologists.
Zare P, Ramezani M.
europepmc +2 more sources
Squamous Cell Carcinoma Transformation of Acrokeratosis Verruciformis of Hopf
Journal of Armed Forces Medical College, Bangladesh, 2019 Acrokeratosis verruciformis of Hopf is a rare genodermatosis with an autosomal dominant mode of inheritance. It is a disorder of keratinization, characterized by multiple, skin-colored keratotic lesions resembling warts typically observed on the dorsum of the hands and feet. Histopathologically, the lesion shows considerable hyperkeratosis, acanthosis,
Md Shirajul Islam Khan
openaire +3 more sources
Clinical and Histopathological Findings in a Patient of Darier-White Disease with Acrokertasosis Verruciformis of Hopf. [PDF]
Case Rep Dermatol Med, 2022 Darier disease (DD) is a rare genodermatoses characterized by greasy hyperkeratotic papules in seborrheic regions and nail and oral changes. Histologically, it presents as suprabasal clefts with acantholytic and dyskeratotic cells. Acrokertasosis verruciformis of Hopf (AKVH) is considered an allelic variant with clinical overlap where Church spires are
Paudel V +3 more
europepmc +2 more sources
Yellowish papules on the palms: a diagnostic challenge. [PDF]
Int J Dermatol, 2023 International Journal of Dermatology, Volume 62, Issue 1, Page 37-39, January 2023.
Maronese CA +5 more
europepmc +2 more sources
Late-onset non-familial acrokeratosis verruciformis of Hopf: a case report.
La Clinica terapeutica, 2019 Acrokeratosis verruciformis of Hopf is a rare heritable autosomal dominant genodermatosis and keratinization disorder, first described in 1931 by Hopf. It presents with multiple flat skin colored papules, mainly localized at the dorsal region of the hands and feet.
Faina V +5 more
openaire +4 more sources
Late onset non-familiar acrokeratosis verruciformis of Hopf
Przegląd Dermatologiczny, 2023 Michelle Alcocer-Salas +2 more
doaj +2 more sources
A Shared Pathogenesis? Elastic Tissue Degeneration in Two Generations: Co-Occurrence of Acrokeratoelastoidosis and ARCL1A Cutis Laxa. [PDF]
Clin Case RepABSTRACT AKE and cutis laxa type ARCL1A are both disorders of elastic fibers characterized histologically by elastin degeneration and/or fragmentation. However, the pathogenesis is thought to be distinct. AKE is an autosomal dominant disorder with an unknown gene mutation.
Alrefaie SI +6 more
europepmc +2 more sources
Indian Journal of Paediatric Dermatology, 2023 Darier disease (DD) and acrokeratosis verruciformis of Hopf are rare autosomal dominant skin disorders. Both are caused by a single gene mutation, i.e., ATP2A2 located on chromosome 12, which is expressed in the skin and brain. However, both the diseases
Avinash Sharma +3 more
doaj +1 more source
Comprehensive Assessment of Dermatologic and Dysmorphic Manifestations in Patients With Down Syndrome. [PDF]
Skin Res TechnolABSTRACT Background Down syndrome (DS), a common chromosomal anomaly caused by trisomy of chromosome 21, is characterized by a broad spectrum of phenotypic characteristics across multiple organ systems, including cardiac defects and leukemia. Dermatological findings are prevalent among individuals with DS; however, these issues are frequently ...
Kaya G, Alavanda C.
europepmc +2 more sources