نتایج جستجو برای: keratoderma

تعداد نتایج: 755  

2012
Renata Elise Tonoli Damiê De Villa Renata Hübner Frainer Luana Pizzarro Meneghello Nelson Ricachnevsky Maurício de Quadros

Olmsted syndrome is a rare congenital, sharply circumscribed transgredient palmoplantar keratoderma. It was first described by Olmsted in 1927. The diagnosis of this rare disease depends on clinical features like symmetrical involvement of keratoderma of the palms and soles and the symmetrical hyperkeratotic plaques around the body orifices. It starts in the neonatal period or in childhood. The...

Journal: :Indian Journal of Dermatology, Venereology and Leprology 2018

Journal: :Indian Journal of Dermatology, Venereology and Leprology 2006

Journal: :British Journal of Dermatology 2017

Journal: :Indian Journal of Dermatopathology and Diagnostic Dermatology 2018

2015
Fahad Almutawa Thusanth Thusaringam Kevin Watters Tenzin Gayden Nada Jabado Denis Sasseville

BACKGROUND Pachyonychia congenita (PC) is a rare autosomal dominant disease whose main clinical features include hypertrophic onychodystrophy and palmoplantar keratoderma. The new classification is based on genetic variants with mutations in keratin KRT6A, KRT6B, KRT6C, KRT16, KRT17, and an unknown mutation. Here, we present a case of PC with unusual clinical and histological features and a fav...

Journal: :journal of dentomaxillofacil radiology, pathology and surgery 0
maryam basirat oro-maxillofacial developmental diseases research center, department of oral medicine, guilan university of medical sciences, dental school, rasht, iran atessa pakfetrat dental research center, mashhad university of medical sciences, dental school, mashhad, iran adineh javadian langaroodi department of oral and maxillofacial radiology, mashhad university of medical sciences, dental school, mashhad, iran

introduction: papillon-lefèvre syndrome(pls) characterized by palmoplantar hyperkeratosis is a rare autosomal recessive genetic disorder with rapidly progressive periodontitis and premature loss of both deciduous and permanent teeth. in this study, we report the clinical and radiographic features of papillon-lefèvre syndrome in an 11- year-old girl and we also discuss the history and various th...

Journal: :Journal of the American Podiatric Medical Association 1987
F J Tomassi J Comerford R A Ransom

Unna-Thost keratoderma is an autosomal dominant inherited disorder of keratinization, with mutation in Keratin 1 gene. The eponym refers specifically to nonepidermolytic keratoderma, although the original Thost family is now known to have had epidermolytic keratoderma. The condition usually presents in the first few months of life and is usually obvious by the age of 4 years. It rarely appears ...

Journal: :Journal of Indian Academy of Oral Medicine and Radiology 2011

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