Journals / İstanbul Kuzey Klinikleri / 2020 / Cilt: 7 - Sayı: 1

A case of hypomelanosis of Ito accompanied by unilateral abnormal limb overgrowth and delayed speech

Pages
71–73
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

Presentation of the current case may be of use in reminding practitioners of the commonextracutaneous findings of HI, along with some rare manifestations, such as delayed speech and asymmetric limb growth.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Hypomelanosis of Ito (HI) is characterized by unilateral or bilateral hypopigmented skin lesions and usually presents as amultisystemic disorder.
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Key Findings & Data:Skin lesions may develop in different textures, such as linear, whorled, or patchy, and are often accompanied by abnormalities of the central nervous system, skeletal system, eyes, and teeth.
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Conclusion & Impact:Presentation of the current case may be of use in reminding practitioners of the commonextracutaneous findings of HI, along with some rare manifestations, such as delayed speech and asymmetric limb growth.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Hypomelanosis of Ito (HI) is characterized by unilateral or bilateral hypopigmented skin lesions and usually presents as amultisystemic disorder. Skin lesions may develop in different textures, such as linear, whorled, or patchy, and are often accompanied by abnormalities of the central nervous system, skeletal system, eyes, and teeth. HI is associated with sporadicgene mutations but not gender. Presentation of the current case may be of use in reminding practitioners of the commonextracutaneous findings of HI, along with some rare manifestations, such as delayed speech and asymmetric limb growth.

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Cite This Article

ÖZÇETİN, M., ÇAĞ, Y., KILIÇ, A., AKSOY, B., BİLGİLİ, F. (2022). A case of hypomelanosis of Ito accompanied by unilateral abnormal limb overgrowth and delayed speech. İstanbul Kuzey Klinikleri, Cilt: 7 - Sayı: 1, 71–73. https://ajindex.com/articles/551369

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References (9)

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