Literature DB >> 26741293

Visual, Ocular Motor, and Cochleo-Vestibular Loss in Patients With Heteroplasmic, Maternally-Inherited Diabetes Mellitus and Deafness (MIDD), 3243 Transfer RNA Mutation.

Simon Cardenas-Robledo1, Ali Saber Tehrani, Gregory Blume, Jorge C Kattah.   

Abstract

BACKGROUND: Mitochondrial encephalopathy, lactic acidosis, and stroke-like symptoms (MELAS) and MIDD (maternally-inherited diabetes mellitus and deafness) are caused by A3243G transfer RNA mutations that affect mitochondrial function. Hearing loss and early onset diabetes mellitus constitute the main MIDD phenotype. Regarding the ophthalmologic manifestations of MIDD, we hypothesized that decreased vestibulo-ocular reflex (VOR) gain in patients with MIDD may contribute to impaired dynamic visual acuity.
METHODS: Neuro-ophthalmologic, neuroimaging, and neuro-otologic evaluations were performed in 2 nonrelated patients with MIDD who complained of oscillopsia with head movement. We obtained quantitative recording of the horizontal and the vertical VOR, using the video head impulse test device.
RESULTS: In the 2 patients, we detected visual, ocular motor, and vestibular abnormalities. Decreased VOR gain in the planes of all 3 semicircular canals and impaired dynamic visual acuity was demonstrated in both cases.
CONCLUSIONS: MIDD patients are primarily recognized by their advanced hearing loss or deafness, early onset diabetes mellitus, and lactic acidosis. Decreased vision in these patients relates primarily to peri-macular retinal atrophy. In addition, loss of vestibular function causes poor dynamic visual acuity. Both patients, in their late fifties, had evidence of progressive central and peripheral nervous system dysfunction.

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Year:  2016        PMID: 26741293     DOI: 10.1097/WNO.0000000000000340

Source DB:  PubMed          Journal:  J Neuroophthalmol        ISSN: 1070-8022            Impact factor:   3.042


  7 in total

1.  The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness.

Authors:  Josef Finsterer; Marlies Frank
Journal:  Oman Med J       Date:  2018-09

2.  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

3.  Eye movement and vestibular dysfunction in mitochondrial A3243G mutation.

Authors:  Sung-Hee Kim; Ziyoda Abdulkhaevna Akbarkhodjaeva; Ileok Jung; Ji-Soo Kim
Journal:  Neurol Sci       Date:  2016-04-13       Impact factor: 3.307

4.  Heteroplasmy Detection of Mitochondrial DNA A3243G Mutation Using Quantitative Real-Time PCR Assay Based on TaqMan-MGB Probes.

Authors:  Enguang Rong; Hanbo Wang; Shujing Hao; Yuhong Fu; Yanyan Ma; Tianze Wang
Journal:  Biomed Res Int       Date:  2018-11-13       Impact factor: 3.246

5.  Vestibular dysfunction: a frequent problem for adults with mitochondrial disease.

Authors:  Sarah Holmes; Amanda J Male; Gita Ramdharry; Cathy Woodward; Natalie James; Iwona Skorupinska; Mariola Skorupinska; Louise Germain; Damian Kozyra; Enrico Bugiardini; Olivia V Poole; Ros Quinlivan; Michael G Hanna; Diego Kaski; Robert D S Pitceathly
Journal:  J Neurol Neurosurg Psychiatry       Date:  2018-11-26       Impact factor: 10.154

Review 6.  The non-syndromic clinical spectrums of mtDNA 3243A>G mutation.

Authors:  Xiya Shen; Ailian Du
Journal:  Neurosciences (Riyadh)       Date:  2021-04       Impact factor: 0.906

7.  Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutations.

Authors:  Liuchun Yang; Qinxian Guo; Jianhang Leng; Keyi Wang; Yu Ding
Journal:  J Clin Lab Anal       Date:  2021-11-22       Impact factor: 2.352

  7 in total

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