A 19-year-old man is presented in order to stress the importance of pachyonychia congenita in the differential diagnosis of subungual and palmoplanter hyperkeratosis in patients vvithout family history.
📌 3 Key Takeaways
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Objective & Hypothesis:Pachyonychia congenita is an ectodermal displasia with autosomal dominant inheritance, of which the most frequent form, Type I (Jadassohn-Lewandowsky syndrome) is characterized by subungual and palmoplanter hyperkeratosis, oral leukokeratosis and follicular keratosis.
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Key Findings & Data:Pachyonychia congenita is an ectodermal displasia with autosomal dominant inheritance, of which the most frequent form, Type I (Jadassohn-Lewandowsky syndrome) is characterized by subungual and palmoplanter hyperkeratosis, oral leukokeratosis and follicular keratosis.
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Conclusion & Impact:A 19-year-old man is presented in order to stress the importance of pachyonychia congenita in the differential diagnosis of subungual and palmoplanter hyperkeratosis in patients vvithout family history.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Pachyonychia congenita is an ectodermal displasia with autosomal dominant inheritance, of which the most frequent form, Type I (Jadassohn-Lewandowsky syndrome) is characterized by subungual and palmoplanter hyperkeratosis, oral leukokeratosis and follicular keratosis. A 19-year-old man is presented in order to stress the importance of pachyonychia congenita in the differential diagnosis of subungual and palmoplanter hyperkeratosis in patients vvithout family history.
Özet
Pakionişi konjenita, en sık görülen formu olan Tip 1 (Jadassohn-Lewandowsky sendromu) subungual ve palmop-lanter hiperkeratoz, oral lökokeratoz ve foliküler keratoz ile karakterize, otozomal dominant kalıtım gösteren bir ek-todermal displazidir. 19 yaşında erkek hasta, aile anamnezinin olmadığı subungual ve palmoplanter hiperkeratoz-lu hastalarda ayırıcı tanıda pakionişi konjenitanın önemini vurgulamak için sunulmuştur.
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Cite This Article
İNANIR, I., UZ, N., AKTAN, Ş., ŞANLI, B. (2022). Pachyonychia congenita: A sporadic case. Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 33 - Sayı: 3, 182–184. https://ajindex.com/articles/622371