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Journals / Samsun Sağlık Bilimleri Dergisi / 2022 / Cilt: 7 Sayı: 3

Audiological Findings in Wolf Hirschhorn Syndrome: A Case Report

WOLF HİRSCHHORN SENDROMUNDA ODYOLOJİK BULGULAR: OLGU SUNUMU

Asuman Küçüköner(ONDOKUZ MAYIS ÜNİVERSİTESİ, SAĞLIK HİZMETLERİ MESLEK YÜKSEKOKULU)0000-0002-4369-727X
Ömer Küçüköner(ONDOKUZ MAYIS ÜNİVERSİTESİ, SAĞLIK BİLİMLERİ FAKÜLTESİ)0000-0002-0262-5093
Pages
987–992
Publication Date
2022-12-30
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AI Summary & Key Takeaways

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

In this article, it is aimed to give information about hearing loss and rehabilitation with a hearing aid in a patient with WHS who has sensorineural hearing loss.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Wolf-Hirschhorn syndrome (WHS) is a contiguous gene disorder clinically characterized by prenatal and postnatal growth deficiency, distinctive craniofacial features, mental retardation, and seizures.
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Key Findings & Data:The disease is caused by partial loss of the distal part of the short arm of chromosome 4.
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Conclusion & Impact:In this article, it is aimed to give information about hearing loss and rehabilitation with a hearing aid in a patient with WHS who has sensorineural hearing loss.
🔬Design:Olgu Sunumu
📍Scope:Comprehensive Sample
⚙️Variables:Wolf-Hirschhorn sendromu · sensörinöral işitme kaybı · işitme cihazı

Abstract

Wolf-Hirschhorn syndrome (WHS) is a contiguous gene disorder clinically characterized by prenatal and postnatal growth deficiency, distinctive craniofacial features, mental retardation, and seizures. The disease is caused by partial loss of the distal part of the short arm of chromosome 4. Although hearing loss has been reported in individuals with WHS in the literature, sensorineural hearing loss is rare. In this article, it is aimed to give information about hearing loss and rehabilitation with a hearing aid in a patient with WHS who has sensorineural hearing loss.

Özet

Wolf-Hirschhorn sendromu (WHS), klinik olarak doğum öncesi ve doğum sonrası büyüme eksikliği, ayırt edici kraniyofasiyal özellikler, mental retardasyon ve nöbetlerle tanımlanan bitişik bir gen bozukluğudur. Hastalığa 4. kromozomun kısa kolunun distal kısmında oluşan kısmi kayıp neden olur. Literatürde WHS'li bireylerde işitme kaybı bildirilmiş olmasına rağmen, sensörinöral işitme kaybı nadirdir. Bu makalede sensörinöral işitme kaybı mevcut olan WHS’li hastanın işitme kaybı ve işitme cihazı ile rehabilitasyonu hakkında bilgi vermek amaçlanmıştır.

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Cite This Article

Küçüköner, A., Küçüköner, Ö. (2022). Audiological Findings in Wolf Hirschhorn Syndrome: A Case Report. Samsun Sağlık Bilimleri Dergisi, Cilt: 7 Sayı: 3, 987–992. https://doi.org/10.47115/jshs.1183343

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