Print ISSN: 2582-4147
Online ISSN: 2582-421X
CODEN : IJOABK
IP Journal of Otorhinolaryngology and Allied Science (JOAS) open access, peer-reviewed quarterly journal publishing since 2018 and is published under the Khyati Education and Research Foundation (KERF), is registered as a non-profit society (under the society registration act, 1860), Government of India with the vision of various accredited vocational courses in healthcare, education, paramedical, yoga, publication, teaching and research activity, with the aim of faster and better dissemination of knowledge, we will be publishing the article more...Case Report
Author Details :
Volume : 5, Issue : 2, Year : 2022
Article Page : 46-49
https://doi.org/10.18231/j.ijoas.2022.012
Abstract
Pachyonychia congenital (PC), is a rare genetic disorder, autosomal dominant, disorder of keratinization. This condition is characterized by cutaneous manifestation mainly hyperkeratosis of skin and mucosae and hypertrophy of nails. In this condition, almost 50% of the patients will have oral leukokeratosis. The case report here is of a 15 years old girl, presented with dystrophic, thickened fingernails and toenails with subungual hyperkeratosis, palmoplantar keratoderma, hyperkeratotic plaques in buccal mucosae. Histological examination shows acanthosis, parakeratosis and ballooning of epithelial cells, these features were consistent leukokeratosis, and has been diagnosed as Pachyonychia Congenita type 1. This is a rare condition hence, has been reported.
Keywords: Follicular papules, Leukokeratosis, Nail dystrophy, Subungual Hyperkeratosis
How to cite : Byahatti N, Oral manifestation of pachyonychia congenita type 1: Jadassohn lewandowsky syndrome. J Otorhinolaryngol Allied Sci 2022;5(2):46-49
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