نتایج جستجو برای: lewandowsky syndrome

تعداد نتایج: 622000  

2011
Ahmad Al Aboud Khalid Al Aboud

Josef Jadassohn (1863-1936) and his assistant, Felix Lewandowsky (1879-1921), were eminent German dermatologists who had several dermatology conditions linked eponymously. One such condition is Jadassohn-Lewandowsky syndrome, which is a type of pachyonychia congenita - a disease that is characterized by severe thickening of the nail due to massive nail hyperkeratosis. This report describes Jada...

Journal: :Indian Journal of Paediatric Dermatology 2014

Journal: :Indian Journal of Dermatology 2015

Journal: :acta medica iranica 0
vitorino modesto dos santos catholic university medical course, brasília-df, brazil . and department of internal medicine, armed forces hospital, brasília-df, brazil. thiago pereira loures department of internal medicine, armed forces hospital, brasília-df, brazil. joão daniel bringel rego division of pneumology, armed forces hospital, brasília-df, brazil. christiane aires teixeira division of pneumology, armed forces hospital, brasília-df, brazil. kayursula dantas de carvalho department of internal medicine, armed forces hospital, brasília-df, brazil. afonso lucas oliveira nascimento department of internal medicine, armed forces hospital, brasília-df, brazil.

pachyonychia congenital (pc) is a rare autosomal dominant genodermatosis characterized hyperkeratosis affecting the nails and palmoplantar areas, oral leukokeratosis, and cystic lesions. a 39-year-old woman with pc type 1 (jadassohn-lewandowsky syndrome) and b-cell lymphoma is described. no similar disorders or parental consanguinity were found in her family. typical features of pc developed si...

2015
Anupama Manohar Prasad Yugandar Inakanti Shiva Kumar

Pachyonychia congenita (PC) is a rare autosomal dominant genodermatosis characterized by hyperkeratosis affecting the nails and palmoplantar areas, oral leucokeratosis, and cystic lesions. It is classically subdivided into two major variants, PC-1 (Jadassohn-Lewandowski syndrome) and PC-2 (Jackson-Lawler syndrome), according to the localization of the mutations in the KRT6A/KRT16 or KRT6B/KRT17...

Journal: :The Journal of Nervous and Mental Disease 1920

2016
Anup Kumar Tiwary Dharmendra Kumar Mishra

PC is commonly described as a rare genodermatosis characteristically manifesting as massive subungual hyperkeratosis with nail thickening, focal palmoplantar keratoderma alongwith deep f issur ing and blistering, oral leukokeratosis and discrete follicular hyperkeratosis [1,2]. Other features including abnormalities of teeth, hairs and larynx can also be seen depending on the clinical types. On...

Journal: :IP Journal of Otorhinolaryngology and Allied Science 2022

Pachyonychia congenital (PC), is a rare genetic disorder, autosomal dominant, disorder of keratinization. This condition characterized by cutaneous manifestation mainly hyperkeratosis skin and mucosae hypertrophy nails. In this condition, almost 50% the patients will have oral leukokeratosis. The case report here 15 years old girl, presented with dystrophic, thickened fingernails toenails subun...

Journal: :Journal of Neurology 2019

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