A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options

N Sharma, D Kumari, I Panigrahi… - Clinical Genetics, 2023 - Wiley Online Library
Hearing impairment is one of the most widespread inheritable sensory disorder affecting at
least 1 in every 1000 born. About two‐third of hereditary hearing loss (HHL) disorders are …

Genetic etiology of non-syndromic hearing loss in Latin America

K Lezirovitz, RC Mingroni-Netto - Human Genetics, 2022 - Springer
Latin America comprises all countries from South and Central America, in addition to
Mexico. It is characterized by a complex mosaic of regions with heterogeneous genetic …

Investigation of GJB2 and SLC26A4 genes related to pendred syndrome genetic deafness patients

HMH Al-Zaidi, F Mousavinasab… - Cellular, Molecular …, 2023 - cmbr-journal.com
Deafness can occur due to damage to the ear, especially the inner ear. In other cases, the
cause is a heterogeneous genetic abnormality and is caused by the changes that occur in …

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss

AC Batissoco, V Pedroso-Campos, E Pardono… - Human genetics, 2022 - Springer
Hearing loss is one of the most common sensory defects, affecting 5.5% of the worldwide
population and significantly impacting health and social life. It is mainly attributed to genetic …

Different Rates of the SLC26A4-Related Hearing Loss in Two Indigenous Peoples of Southern Siberia (Russia)

VY Danilchenko, MV Zytsar, EA Maslova… - Diagnostics, 2021 - mdpi.com
Hereditary hearing loss (HL) is known to be highly locus/allelic heterogeneous, and the
prevalence of different HL forms significantly varies among populations worldwide …

Assessment of the clinical benefit of imaging in children with unilateral sensorineural hearing loss: a systematic review and meta-analysis

FG Ropers, ENB Pham, SG Kant… - … –Head & Neck …, 2019 - jamanetwork.com
Importance Imaging used to determine the cause of unilateral sensorineural hearing loss
(USNHL) in children is often justified by the high likelihood of detecting abnormalities, which …

[HTML][HTML] SLC26A4 基因在大前庭水管综合征和/或Mondini 畸形患儿中突变频率的观察

刘亚青, 黄正华, 孙晨, 沈小飞, 李伟… - Journal of Clinical …, 2021 - ncbi.nlm.nih.gov
SLC26A4基因在大前庭水管综合征和/或Mondini畸形患儿中突变频率的观察- PMC Back to Top
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A novel method for detecting nine hotspot mutations of deafness genes in one tube

Y Yu, J Zhang, Y Zhan, G Luo - Scientific Reports, 2024 - nature.com
Deafness is a common sensory disorder. In China, approximately 70% of hereditary
deafness originates from four common deafness-causing genes: GJB2, SLC26A4, GJB3 …

Inhibiting SLC26A4 reverses cardiac hypertrophy in H9C2 cells and in rats

L Tang, X Yu, Y Zheng, N Zhou - PeerJ, 2020 - peerj.com
Background It has been confirmed that mutations in solute carrier family 26 member 4
(SLC26A4) contribute to pendred syndrome. However, the role of SLC26A4 in cardiac …

Downregulation of GJB2 and SLC26A4 genes induced by noise exposure is associated with cochlear damage

AA Garmaroudi, M Khadem, MM Hotkani… - Molecular Biology …, 2022 - Springer
Background Noise-induced hearing loss (NIHL) is one the major causes of acquired hearing
loss in developed countries. Noise can change the pattern of gene expression, inducing …