Pachyonychia congenita type-1 (Jadassohn-Lewandowsky syndrome)

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Jadassohn Lewandowsky syndrome: Type 1 pachyonychia congenita

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Josef Jadassohn (1863–1936), Felix Lewandowsky (1879–1921), and their syndrome

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...

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Jadassohn Lewandowsky Syndrome: A Rare Entity

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...

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Acro-osteolysis: a complication of Jadassohn-Lewandowsky syndrome.

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ژورنال

عنوان ژورنال: Indian Journal of Paediatric Dermatology

سال: 2014

ISSN: 2319-7250

DOI: 10.4103/2319-7250.143675