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

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

Sayfa
71–73
Yayın Tarihi
2022-10-18
DOI
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

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 Maddede Bu Makale

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Amaç & Hipotez:Hypomelanosis of Ito (HI) is characterized by unilateral or bilateral hypopigmented skin lesions and usually presents as amultisystemic disorder.
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Temel Bulgular & Veri: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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Sonuç & Katkı: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.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

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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Bu Makaleye Atıf Yap

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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Kaynakça (9)

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  2. Ruggieri M, Pavone L. Hypomelanosis of Ito: clinical syndrome or just phenotype? J Child Neurol 2000;15:635–44
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  6. Molho-Pessach V, Schaffer JV. Blaschko lines and other patterns of cutaneous mosaicism. Clin Dermatol 2011;29:205–25
  7. Küster W, König A. Hypomelanosis of Ito: no entity, but a cutaneous sign of mosaicism. Am J Med Genet 1999;85:346–50
  8. Ruiz-Maldonado R, Toussaint S, Tamayo L, Laterza A, del Castillo V. Hypomelanosis of Ito: diagnostic criteria and report of 41 cases. Pediatr Dermatol 1992;9:1–10
  9. Ream M. Hypomelanosis of Ito. In: Neurocutaneous syndromes, Handbook of clinical neurology, Islam MP, Roach ES, editors. Vol. 132. 1st ed.Amsterdam: Elsevier; 2015. p. 281–7.