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Journals / Türkderm-Deri Hastalıkları ve Frengi Arşivi / 2008 / Cilt: 42 - Sayı: 4

Ichthyosis vulgaris coexisted with acrokeratosis verruciformis: A case report

İktiyozis vulgaris ve akrokeratozis verrüsiformis birlikteliği: Bir olgu sunumu

Didem Didar BALCI
Gamze SERARSKAN
Esin ATİK
Pages
134–136
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We present a case of ichthyosis vulgaris coexisted with acrokeratosis verruciformis in a 24-year-old woman.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Ichthyosis vulgaris is an autosomal dominant inherited, keratinization disorder and characterized by diffuse scaling.
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Key Findings & Data:Acrokeratosis verruciformis is also an autosomal dominant, rare keratinization disorder and characterized by warty, brownish to skin colored papules on the dorsa of the hands and feet.
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Conclusion & Impact:We present a case of ichthyosis vulgaris coexisted with acrokeratosis verruciformis in a 24-year-old woman.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Ichthyosis vulgaris is an autosomal dominant inherited, keratinization disorder and characterized by diffuse scaling. Acrokeratosis verruciformis is also an autosomal dominant, rare keratinization disorder and characterized by warty, brownish to skin colored papules on the dorsa of the hands and feet. We present a case of ichthyosis vulgaris coexisted with acrokeratosis verruciformis in a 24-year-old woman.

Özet

İktiyozis vulgaris, otozomal dominant geşiş gösteren bir keratinizasyon hastalığıdır ve yaygın pullanma ile karakterizedir. Akrokeratozis verrusiformis de otozomal dominant, nadir görülen bir keratinizasyon hastalığı olup, el ve ayak dorsal yüzde siğilimsi, kahverengi-deri renginde papüller ile karakterizedir. Burada, iktiyozis vulgaris ve akrokeratozis verrüsiformisin bir arada olduğu, 24 yaşında bir bayan hastayı sunmaktayız

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Cite This Article

BALCI, D. D., SERARSKAN, G., ATİK, E. (2022). Ichthyosis vulgaris coexisted with acrokeratosis verruciformis: A case report. Türkderm-Deri Hastalıkları ve Frengi Arşivi, Cilt: 42 - Sayı: 4, 134–136. https://ajindex.com/articles/622098

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References (10)

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