Results 31 to 40 of about 4,726 (248)
Clinical Efficacy of Potassium Hydroxide 10% for the Treatment of Common Warts [PDF]
International Journal of Medical Arts, 2022 Background and Aim: Common wart is considered one of the common diseases that are caused by the human papillomavirus; despite the high tendency for spontaneous recovery, it needs treatment. Topical application of keratolytic agent on virus-infected cells
Mahmoud Makki +2 more
doaj +1 more source
Psoriasis part 2 – topical treatment, phototherapy and skin care [PDF]
Farmacja Polska, 2023 Psoriasis is a chronic inflammatory disease that requires the selection of appropriate pharmacotherapy and skin care. Topical treatment should be added in pharmacotherapy of every patient with psoriasis.
Ewa Zwierzyńska +2 more
doaj +1 more source
Moisturizing and Keratolytic Agents [PDF]
, 2012 Raquel Pardavila Riveiro and Celia Posada García
openalex +2 more sources
Response of papillon–Lefevre syndrome to acitretin
Indian Journal of Paediatric Dermatology, 2021 Papillon–Lefevre (PLS) is a rare autosomal recessive disorder of keratinization characterized by symmetric, trans-gradient type palmoplantar keratoderma (PPK), rapidly progressive periodontopathy, and precocious loss of dentition.
Priyanka Arun Kowe +3 more
doaj +1 more source
Excellent response to adalimumab in a patient with Papillon–Lefèvre syndrome: A case report
JEADV Clinical Practice, 2023 Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disease that presents clinically with palmoplantar keratoderma and periodontitis and results in early‐onset dental loss. PLS management is difficult.
Eman Almukhadeb +4 more
doaj +1 more source
Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient [PDF]
Anais Brasileiros de Dermatologia, 2014 Buschke-Fisher-Brauer keratoderma is a rare hereditary autosomal dominant disease of incomplete penetrance. Important differential diagnoses include other palmoplantar keratinization disorders, acquired or hereditary, which is done based on the ...
João Roberto Antonio +3 more
doaj +2 more sources
Indian Journal of Dermatology, 2021 We report a case of annular epidermolytic ichthyosis (AEI) resulting from de novo keratin 1 gene mutation. AEI is a rare autosomal dominantly inherited cornification disorder and is a distinct phenotypic variant of bullous congenital ichthyosiform ...
Lihong Chen +4 more
doaj +1 more source
Ungulomycosis of cattle: etiological factors and pathogenetic mechanisms
Науковий вісник Львівського національного університету ветеринарної медицини та біотехнологій імені С.З. Ґжицького: Серія Ветеринарні науки, 2021 Mycotic diseases, ie those caused by microscopic fungi, are widespread among animals. As for cattle, at present ungulomycosis has become the most widespread, in which keratolytic fungi affect the hooves of animals, causing complications such as ...
Y. G. Krupnyk +2 more
doaj +1 more source
A case of peeling skin syndrome
Indian Dermatology Online Journal, 2017 Peeling skin syndrome is a very rare autosomal recessive disease characterized by widespread painless peeling of the skin in superficial sheets. Etiology is still unknown with an autosomal recessive inheritance.
Anil K Singhal +3 more
doaj +1 more source
Profile of clindamycin phosphate 1.2%/benzoyl peroxide 3.75% aqueous gel for the treatment of acne vulgaris. [PDF]
, 2015 Acne vulgaris is a common and chronic skin disease, and is a frequent source of morbidity for affected patients. Treatment of acne vulgaris is often difficult due to the multifactorial nature of this disease.
Eichenfield, Lawrence F, Nguyen, Tuyet A
core +2 more sources