Results 1 to 10 of about 47,809 (336)

Acrokeratosis verruciformis of Hopf: A rare presentation in a young Indian female—A case report and review [PDF]

open access: yesJournal of Family Medicine and Primary Care
Acrokeratosis 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

Epidermolytic hyperkeratosis with rickets

open access: goldIndian Journal of Dermatology, Venereology and Leprology, 2006
A 6-year-old child presented with generalized hyperkeratosis, most marked over the flexures; windswept deformity of the legs; and limping since 3 years. On the basis of the clinical, histopathologic and biochemical findings, he was diagnosed as a case of epidermolytic hyperkeratosis with rickets.
Surajit Nayak   +4 more
openaire   +4 more sources

Bethlem myopathy: An autosomal dominant myopathy with flexion contractures, keloids, and follicular hyperkeratosis

open access: diamondAnnals of Indian Academy of Neurology, 2013
Bethlem myopathy and Ullrich congenital muscular dystrophy form a spectrum of collagenopathies caused by genetic mutations encoding for any of the three subunits of collagen VI.
A. Saroja   +3 more
semanticscholar   +2 more sources

Erythematous Papules with Central Hyperkeratosis in Two Young Women: A Quiz [PDF]

open access: yesActa Dermato-Venereologica
is missing (Quiz)
Nadine Wiedenmayer   +3 more
doaj   +2 more sources

EPCAM and TROP2 share a role in claudin stabilization and development of intestinal and extraintestinal epithelia in mice

open access: yesBiology Open, 2022
Epithelial cell adhesion molecule (EPCAM) is a transmembrane glycoprotein expressed on the surface of most epithelial and epithelium-derived tumor cells and reported to regulate stability of epithelial tight junction proteins, claudins.
Roman Szabo   +3 more
doaj   +1 more source

Epidermolytic hyperkeratosis of the vulva [PDF]

open access: yesDermatology Online Journal, 2021
Vulvar epidermolytic hyperkeratosis is a benign entity that mimics other malignant and inflammatory vulvar dermatoses clinically and histologically requiring careful clinical pathologic correlation for diagnosis.
Dai, Christina   +4 more
openaire   +5 more sources

Papillon-Lefevre Syndrome In An Adolescent Female: A Case Study [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Papillon-Lefevre Syndrome (PLS) is a rare inherited autosomal-recessive condition with one-third of the patients’ showing consanguinity of the parents. Lesions are characterised by palmar-plantar hyperkeratosis and hyperhidrosis.
M.J. Jijin   +4 more
doaj   +1 more source

Post-Pemphigus Acanthomata Presenting as an Isolated, Hyperkeratotic Plaque

open access: yesDermatopathology, 2023
Post-pemphigus acanthomas have been rarely discussed in the literature. A prior case series identified 47 cases of pemphigus vulgaris and 5 cases of pemphigus foliaceus, out of which 13 developed acanthomata as a part of the healing process. Additionally,
Rachita Pandya   +4 more
doaj   +1 more source

Clinical and histopathological study of cutaneous lichen planus in a tertiary care center of central India

open access: yesMGM Journal of Medical Sciences, 2023
Background: Lichen planus (LP) is an idiopathic, chronic inflammatory disease of the skin, mucous membrane, and nails. Worldwide distribution is seen, with 0.38% of the lesions prevalent in India.
Suvidhi Wankhade   +3 more
doaj   +1 more source

Epidermolytic Hyperkeratosis

open access: yesDefinitions, 2020
Epidermolytic hyperkeratosis can be categorized into two types. People with PS-type epidermolytic hyperkeratosis have thick skin on the palms of their hands and soles of their feet (palmoplantar or palm/sole hyperkeratosis) in addition to other areas of ...
Epidermolytic hyperkeratosis
semanticscholar   +1 more source

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