Mitochondrial Sensorineural Hearing Loss: A Retrospective Study and a Description of Cochlear Implantation in a MELAS Patient.

Q3 Biochemistry, Genetics and Molecular Biology
Genetics Research International Pub Date : 2012-01-01 Epub Date: 2012-02-20 DOI:10.1155/2012/287432
Mauro Scarpelli, Francesca Zappini, Massimiliano Filosto, Anna Russignan, Paola Tonin, Giuliano Tomelleri
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引用次数: 25

Abstract

Hearing impairment is common in patients with mitochondrial disorders, affecting over half of all cases at some time in the course of the disease. In some patients, deafness is only part of a multisystem disorder. By contrast, there are also a number of "pure" mitochondrial deafness disorders, the most common probably being maternally inherited. We retrospectively analyzed the last 60 genetically confirmed mitochondrial disorders diagnosed in our Department: 28 had bilateral sensorineural hearing loss, whereas 32 didn't present ear's abnormalities, without difference about sex and age of onset between each single group of diseases. We reported also a case of MELAS patient with sensorineural hearing loss, in which cochlear implantation greatly contributed to the patient's quality of life. Our study suggests that sensorineural hearing loss is an important feature in mitochondrial disorders and indicated that cochlear implantation can be recommended for patients with MELAS syndrome and others mitochondrial disorders.

Abstract Image

线粒体感音神经性听力损失:MELAS患者人工耳蜗植入的回顾性研究和描述。
听力障碍在线粒体疾病患者中很常见,在疾病过程中的某个时间影响了一半以上的病例。在一些患者中,耳聋只是多系统疾病的一部分。相比之下,也有一些“纯”线粒体耳聋疾病,最常见的可能是母系遗传。我们回顾性分析了最近60例在我科诊断的遗传证实的线粒体疾病:28例为双侧感音神经性听力损失,32例未出现耳部异常,每组疾病在性别和发病年龄上无差异。我们也报告了一例MELAS合并感音神经性听力损失的患者,其中人工耳蜗植入对患者的生活质量有很大的帮助。我们的研究表明,感音神经性听力损失是线粒体疾病的一个重要特征,并提示对于MELAS综合征和其他线粒体疾病患者可以推荐人工耳蜗植入。
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来源期刊
Genetics Research International
Genetics Research International Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.90
自引率
0.00%
发文量
0
期刊介绍: Genetics Research International is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of genetics and genomics. The journal focuses on articles bearing on heredity, biochemistry, and molecular biology, as well as clinical findings.
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