Literature DB >> 27359089

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

V P Vandana1, Parayil Sankaran Bindu2, Kothari Sonam3, Periyasamy Govindaraj4, Arun B Taly5, Narayanappa Gayathri6, Shwetha Chiplunkar7, Chikkanna Govindaraju8, H R Arvinda9, Madhu Nagappa10, Sanjib Sinha11, Kumarasamy Thangaraj12.   

Abstract

OBJECTIVES: Reports of audiological manifestations in specific subgroups of mitochondrial disorders are limited. This study aims to describe the audiological findings in patients with MELAS syndrome and m.3243A>G mutation. PATIENTS &
METHODS: Audiological evaluation was carried out in eight patients with confirmed MELAS syndrome and m.3243A>G mutation. The evaluation included a complete neurological evaluation, pure tone audiometry (n=8), otoacoustic emissions (n=8) and brainstem evoked response audiometry (n=6), magnetic resonance imaging (n=8) and muscle biospy (n=6).
RESULTS: Eight patients (Age range: 5-45 years; M:F-1:3) including six children and two adults underwent formal audiological evaluation. Five patients had hearing loss; of these two had "subclinical hearing loss", one had moderate and two had severe hearing loss. The abnormalities included abnormal audiometry (n=5), otoacoustic emission testing (n=7) and absent brainstem auditory evoked responses (n=1). The findings were suggestive of cochlear involvement in four and retrocochlear in one.
CONCLUSIONS: This study shows that hearing loss of both cochlear and retrocochlear origin occurs in patients with MELAS and may be subclinical. Early referrals for audiological evaluation is warranted to recognize the subclinical hearing loss in these patients. The therapeutic implications include early interventions in the form of hearing aids, cochlear implants and cautioning the physicians for avoidance of aminoglycosides.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Auditory neuropathy; MELAS; Sensory neural deafness; m.3243A>G

Mesh:

Year:  2016        PMID: 27359089     DOI: 10.1016/j.clineuro.2016.04.024

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  10 in total

1.  Audiological and Vestibular Findings in Subjects with MELAS Syndrome.

Authors:  Dan Dupont Hougaard; Danial Hofgaard Hestoy; Allan Thomas Hojland; Michael Gailhede; Michael Bjorn Petersen
Journal:  J Int Adv Otol       Date:  2019-08       Impact factor: 1.017

2.  Cochlear Implantation in Patients with Mitochondrial Gene Mutation: Decline in Speech Perception in Retrospective Long-Term Follow-Up Study.

Authors:  Kai Kanemoto; Akinori Kashio; Erika Ogata; Yusuke Akamatsu; Hajime Koyama; Tsukasa Uranaka; Yujiro Hoshi; Shinichi Iwasaki; Tatsuya Yamasoba
Journal:  Life (Basel)       Date:  2022-03-26

3.  Rapid Detection of the mt3243A > G Mutation Using Urine Sediment in Elderly Chinese Type 2 Diabetic Patients.

Authors:  Yinan Zhang; Xiujuan Du; Xinqian Geng; Chen Chu; Huijuan Lu; Yixie Shen; Ruihua Chen; Pingyan Fang; Yanmei Feng; Xiaojie Zhang; Yan Chen; Yanping Zhou; Congrong Wang; Weiping Jia
Journal:  J Diabetes Res       Date:  2017-06-21       Impact factor: 4.011

4.  Hearing impairment in MELAS: new prospective in clinical use of microRNA, a systematic review.

Authors:  Arianna Di Stadio; Valentina Pegoraro; Laura Giaretta; Laura Dipietro; Roberta Marozzo; Corrado Angelini
Journal:  Orphanet J Rare Dis       Date:  2018-02-21       Impact factor: 4.123

5.  Temporal bone histopathology in MELAS syndrome.

Authors:  Ophir Handzel; Omer J Ungar; Dan J Lee; Joseph B Nadol
Journal:  Laryngoscope Investig Otolaryngol       Date:  2020-01-07

6.  Long-Term Progression and Rapid Decline in Hearing Loss in Patients with a Point Mutation at Nucleotide 3243 of the Mitochondrial DNA.

Authors:  Aki Sakata; Akinori Kashio; Hajime Koyama; Tsukasa Uranaka; Shinichi Iwasaki; Chisato Fujimoto; Makoto Kinoshita; Tatsuya Yamasoba
Journal:  Life (Basel)       Date:  2022-04-06

7.  Effects of CoQ10 Replacement Therapy on the Audiological Characteristics of Pediatric Patients with COQ6 Variants.

Authors:  Dong Woo Nam; Sang Soo Park; So Min Lee; Myung-Whan Suh; Moo Kyun Park; Jae-Jin Song; Byung Yoon Choi; Jun Ho Lee; Seung Ha Oh; Kyung Chul Moon; Yo Han Ahn; Hee Gyung Kang; Hae Il Cheong; Ji Hyun Kim; Sang-Yeon Lee
Journal:  Biomed Res Int       Date:  2022-09-09       Impact factor: 3.246

Review 8.  Recent advances in mitochondrial diseases: From molecular insights to therapeutic perspectives.

Authors:  Ahmad M Aldossary; Essam A Tawfik; Mohammed N Alomary; Samar A Alsudir; Ahmed J Alfahad; Abdullah A Alshehri; Fahad A Almughem; Rean Y Mohammed; Mai M Alzaydi
Journal:  Saudi Pharm J       Date:  2022-05-28       Impact factor: 4.562

9.  Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report.

Authors:  Ahmad F Alenezi; Mariam A Almelahi; Feten Fekih-Romdhana; Haitham A Jahrami
Journal:  J Med Case Rep       Date:  2022-10-10

Review 10.  Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome: A case-report and literature review (CARE-complaint).

Authors:  Shuai Wang; Tao Song; Suping Wang
Journal:  Medicine (Baltimore)       Date:  2020-06-12       Impact factor: 1.817

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.