【佳學基因檢測】前庭功能障礙基因檢測Vestibular dysfunction

基因檢測機構介紹：

基因檢測單位名稱：新疆維吾爾自治區(qū)烏魯木齊市基因檢測研究所。其他成熟基因檢測項目：循環(huán)IgG亞型增加地貧基因檢測結(jié)果分析, 淋巴細胞凋亡異常高通量基因檢測結(jié)果是這樣的！。耳鼻喉科致病基因鑒定基因解碼的研究數(shù)據(jù)表明內(nèi)耳負責聽力和平衡。 這些功能取決于機械敏感毛細胞的正確功能，這些毛細胞將聲音和運動引起的刺激轉(zhuǎn)化為傳送到大腦的電信號。 在內(nèi)耳的進化過程中，聽覺器官發(fā)生了重大變化，而同期所有脊椎動物的前庭器官結(jié)構保持不變。 由于多種交叉原因：遺傳、環(huán)境因素、耳毒性藥物、感染和衰老，前庭功能障礙在人類中非常普遍。 對與平衡缺陷相關的耳聾基因及其相應動物模型的研究揭示了這兩種感覺系統(tǒng)的發(fā)育和功能。 雙側(cè)前庭功能障礙通常會損害個體姿勢控制、凝視穩(wěn)定、運動和空間定向。 由此產(chǎn)生的頭暈、眩暈和/或跌倒（在老年人群中很常見）極大地影響了患者的生活質(zhì)量。 在沒有治療的情況下，前庭植入物等假肢裝置正在開發(fā)中，可提供有關身體運動的方向、幅度和速度的信息，并在動物模型和人類身上取得了可喜的成果。 新的方法和技術已導致針對內(nèi)耳的基因療法（基因補充和基因編輯）、3D 內(nèi)耳類器官和用于生成毛細胞樣細胞的重編程方案取得重大進展。 涵蓋基礎研究、臨床診斷和治療的多尺度方法的這些快速進步正在促進跨學科研究，以開發(fā)針對前庭疾病的個性化治療。

基因檢測導讀：

前庭功能障礙基因檢測的簡單介紹: 來自北京市市轄區(qū)豐臺區(qū)宛平城地區(qū)的郭偉倫（化名）在廣西民族醫(yī)院南寧地區(qū)人民醫(yī)院被醫(yī)生診斷為前庭功能障礙?！禔dvances in Oto-Rhino-Laryngology》臨床討化，前庭功能障礙的出現(xiàn)有多種原因，其中一個重要的原因是基因突變，這需要通過基因檢測來明確。基因突變引起的可能會遺傳。

本文關鍵詞

前庭,功能障礙,基因檢測

人體疾病表征數(shù)據(jù)庫查詢

產(chǎn)生前庭功能障礙醫(yī)師會懷疑以下疾病類型：

怎樣才能診斷準確？

HP:0001751

表型描述

An abnormality of the functioning of the vestibular apparatus.The inner ear is responsible for both hearing and balance. These functions are dependent on the correct functioning of mechanosensitive hair cells, which convert sound- and motion-induced stimuli into electrical signals conveyed to the brain. During evolution of the inner ear, the major changes occurred in the hearing organ, whereas the structure of the vestibular organs remained constant in all vertebrates over the same period. Vestibular deficits are highly prevalent in humans, due to multiple intersecting causes: genetics, environmental factors, ototoxic drugs, infections and aging. Studies of deafness genes associated with balance deficits and their corresponding animal models have shed light on the development and function of these two sensory systems. Bilateral vestibular deficits often impair individual postural control, gaze stabilization, locomotion and spatial orientation. The resulting dizziness, vertigo, and/or falls (frequent in elderly populations) greatly affect patient quality of life. In the absence of treatment, prosthetic devices, such as vestibular implants, providing information about the direction, amplitude and velocity of body movements, are being developed and have given promising results in animal models and humans. Novel methods and techniques have led to major progress in gene therapies targeting the inner ear (gene supplementation and gene editing), 3D inner ear organoids and reprograming protocols for generating hair cell-like cells. These rapid advances in multiscale approaches covering basic research, clinical diagnostics and therapies are fostering interdisciplinary research to develop personalized treatments for vestibular disorders.

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