Results 21 to 30 of about 1,348 (172)
Toenail onychodystrophy of the diabetic foot [PDF]
BMJ Case Reports, 2012 A 54-year-old diabetic female patient with type 2 diabetes of 7 years’ duration presented with pain in her big toe. She had previously sustained foot ulceration several times and hence worried for recurrence. On examination she had a laminated, thickened, dark yellow toe nail of an extremely rare structure (figure1).
Mesut, Mutluoglu +2 more
openaire +2 more sources
Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
Indian Dermatology Online Journal, 2013 Dermatopathia pigmentosa reticularis is a rare ectodermal dysplasia with a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Vinay Shanker, Mudita Gupta
doaj +1 more source
Nail psoriasis: dynamics of the clinical course during anti-IL-17 therapy
Медицинский совет, 2022 Psoriasis is a chronic immune-mediated inflammatory disease in which the pathological process quite often involves the nail apparatus. Psoriatic onychodystrophy is considered a serious psychological and social problem, as nail lesions are not only a ...
O. V. Zhukova +2 more
doaj +1 more source
Netakimab in the therapy of psoriatic onychodystrophy
Медицинский совет, 2022 Psoriatic onychodystrophy affects up to 50% of patients with psoriasis and up to 80% of patients with psoriatic arthritis, with an estimated lifetime risk of nail plate changes in this patient population of up to 90%. Nail psoriasis is characterised by a
O. V. Zhukova +3 more
doaj +1 more source
Vestnik Dermatologii i Venerologii, 2020 Psoriasis is a chronic immune-mediated disease with predominant damage to the skin and musculoskeletal system. This paper describes the clinical manifestations of psoriasis requiring a special therapeutic approach.
Alexander S. Zhukov +3 more
doaj +1 more source
Indian Journal of Dermatology, 2022 DOORS syndrome is an autosomal recessive genetic neurometabolic disorder. It occurs equally in men and women. Major causes include TBC1D 24 mutations and genetic factors.
Dua Cebeci, Didem Rıfkı
doaj +1 more source
Clinical, Cosmetic and Investigational Dermatology, 2023 Anon Paichitrojjana School of Anti-Aging and Regenerative Medicine, Mae Fah Luang University, Bangkok, ThailandCorrespondence: Anon Paichitrojjana, School of Anti-Aging and Regenerative Medicine, Mae Fah Luang University 36/87-88 PS Tower 25Fl, Asoke ...
Paichitrojjana A
doaj
Hypersensitivity in a dog accompanied by generalised onychodystrophy [PDF]
Veterinarski Glasnik, 2018 Canine food hypersensitivity and canine atopic dermatitis are two of the most common allergic diseases in dogs. Food hypersensitivity is typically non-seasonal reaction of types I, III and IV, directed most commonly against glycoproteins in the foods ...
Kotnik Tina
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Oligogenic inheritance in epilepsy: A systematic exome‐wide analysis
Epilepsia, EarlyView.Abstract Objective Genetic factors contribute to the majority of epilepsies, but the exact genetic cause remains unknown in most patients. Incomplete penetrance and variable expressivity are frequent, and recent studies showed a burden of deleterious variants in epilepsy genes, suggesting a role for oligogenic inheritance.
Sarah Duerinckx +192 more
wiley +1 more source
Alopecia Areata in a Patient Receiving Cemiplimab for Metastatic Cutaneous Squamous Cell Carcinoma
JEADV Clinical Practice, EarlyView.ABSTRACT Introduction Alopecia areata (AA) is an autoimmune disease characterized by non‐scarring hair loss of the scalp and/or body, with an unpredictable and variable clinical course. Its etiology is not entirely understood, although evidence suggests that environmental, immunological, and genetic factors contribute to disease development.
Marco Rubatto +7 more
wiley +1 more source