Cargando…

Characterization of vertigo and hearing loss in patients with Fabry disease

BACKGROUND: Fabry Disease (FD) is an X-linked hereditary lysosomal storage disorder which leads to a multisystemic intralysosomal accumulation of globotriaosylceramid (Gb3). Besides prominent renal and cardiac organ involvement, patients commonly complain about vestibulocochlear symptoms like high-f...

Descripción completa

Detalles Bibliográficos
Autores principales:	Köping, Maria, Shehata-Dieler, Wafaa, Schneider, Dieter, Cebulla, Mario, Oder, Daniel, Müntze, Jonas, Nordbeck, Peter, Wanner, Christoph, Hagen, Rudolf, Schraven, Sebastian P.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6094894/ https://www.ncbi.nlm.nih.gov/pubmed/30111353 http://dx.doi.org/10.1186/s13023-018-0882-7

Ejemplares similares

Cardiac and renal dysfunction is associated with progressive hearing loss in patients with Fabry disease
por: Köping, Maria, et al.
Publicado: (2017)

Hot topics in Fabry disease
por: Cairns, Tereza, et al.
Publicado: (2018)

Treatment of hypertrophic cardiomyopathy caused by cardiospecific variants of Fabry disease with chaperone therapy
por: Müntze, Jonas, et al.
Publicado: (2018)

Association and diagnostic utility of diastolic dysfunction and myocardial fibrosis in patients with Fabry disease
por: Liu, Dan, et al.
Publicado: (2018)

Oral Chaperone Therapy Migalastat for Treating Fabry Disease: Enzymatic Response and Serum Biomarker Changes After 1 Year
por: Müntze, Jonas, et al.
Publicado: (2019)

Value of the CHA(2)DS(2)-VASc score and Fabry-specific score for predicting new-onset or recurrent stroke/TIA in Fabry disease patients without atrial fibrillation
por: Liu, Dan, et al.
Publicado: (2018)

Response to “Oral Chaperone Therapy Migalastat for the Treatment of Fabry Disease: Potentials and Pitfalls of Real‐World Data”
por: Müntze, Jonas, et al.
Publicado: (2019)

Case report of a 45-year old female Fabry disease patient carrying two alpha-galactosidase A gene mutation alleles
por: Oder, Daniel, et al.
Publicado: (2016)

Hereditary hearing loss SNP-microarray pilot study
por: Vona, Barbara, et al.
Publicado: (2018)

Organ manifestations and long-term outcome of Fabry disease in patients with the GLA haplotype D313Y
por: Oder, Daniel, et al.
Publicado: (2016)

High-sensitivity FEES(®) with the professional image enhancement technology “PIET”
por: Kraus, Fabian, et al.
Publicado: (2021)

Clinical impact of the alpha-galactosidase A gene single nucleotide polymorphism -10C>T: A single-center observational study
por: Oder, Daniel, et al.
Publicado: (2018)

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations
por: Vona, Barbara, et al.
Publicado: (2014)

X‐chromosomal inactivation patterns in women with Fabry disease
por: Wagenhäuser, Laura, et al.
Publicado: (2022)

Hearing loss in children with Fabry disease
por: Suntjens, E., et al.
Publicado: (2017)

Long‐term outcome after surgical repair of a rapid‐grown ischemic ventricular aneurysm causing ventricular tachycardia
por: Gensler, Daniel, et al.
Publicado: (2019)

Endolymphatic Hydrops in Fluctuating Hearing Loss and Recurrent Vertigo
por: Domínguez, Pablo, et al.
Publicado: (2021)

A Case Study Assessing the Auditory and Speech Development of Four Children Implanted with Cochlear Implants by the Chronological Age of 12 Months
por: May-Mederake, Birgit, et al.
Publicado: (2013)

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
por: Vona, Barbara, et al.
Publicado: (2014)

Contrast-enhanced ultrasound for non-invasive differential diagnosis of unclear left atrial mass
por: Christa, Martin, et al.
Publicado: (2023)

High‐Sensitivity Troponin: A Clinical Blood Biomarker for Staging Cardiomyopathy in Fabry Disease
por: Seydelmann, Nora, et al.
Publicado: (2016)

Patterns of nystagmus conversion in sudden sensorineural hearing loss with vertigo
por: Kim, Chang-Hee, et al.
Publicado: (2018)

Vertigo and hearing loss during the COVID-19 pandemic – is there an association?
por: Karimi-Galougahi, Mahboobeh, et al.
Publicado: (2021)

Association between Comorbidities and Progression of Transvalvular Pressure Gradients in Patients with Moderate and Severe Aortic Valve Stenosis
por: Salinger, Tim, et al.
Publicado: (2018)

What Is the Role of Sensorineural Hearing Loss in Fabry Disease Screening?
por: Köroğlu, Ekin Yiğit, et al.
Publicado: (2023)

Functional and Molecular Markers for Hearing Loss and Vertigo Attacks in Meniere’s Disease
por: Yang, Chao-Hui, et al.
Publicado: (2023)

Association Between Hearing Characteristics/Prognosis and Vestibular Function in Sudden Sensorineural Hearing Loss With Vertigo
por: Wang, Yixu, et al.
Publicado: (2020)

Artificial Neural Network-Assisted Classification of Hearing Prognosis of Sudden Sensorineural Hearing Loss With Vertigo
Publicado: (2023)

Middle-ear effusion in children with cleft palate: congenital or acquired?
por: Kraus, F, et al.
Publicado: (2022)

Genetics of Tinnitus: Still in its Infancy
por: Vona, Barbara, et al.
Publicado: (2017)

Association of Fabry Disease with Hearing Loss, Tinnitus, and Sudden Hearing Loss: A Nationwide Population-Based Study
por: Cheng, Yen-Fu, et al.
Publicado: (2022)

Gene variants of unknown significance in Fabry disease: Clinical characteristics of c.376A>G (p.Ser126Gly)
por: Lau, Kolja, et al.
Publicado: (2022)

Vestibular Aqueduct Morphology and Meniere's Disease—Development of the “Vestibular Aqueduct Score” by 3D Analysis
por: Noyalet, Laurent, et al.
Publicado: (2022)

Sudden Hearing Loss and Vertigo With Silent Pontine Infarction: A Case Report
por: Jeong, Jae Yeong, et al.
Publicado: (2023)

Investigation of hearing loss in elderly vertigo and dizziness patients in the past 10 years
por: Wang, Qian, et al.
Publicado: (2023)

Subacute carbon monoxide poisoning presenting as vertigo and fluctuating low frequency hearing loss
por: Seale, Bethany, et al.
Publicado: (2018)

Contribution of Audiogram Classification in Evaluating Vestibular Dysfunction in Sudden Sensorineural Hearing Loss With Vertigo
por: Jiang, Zhuang, et al.
Publicado: (2021)

Early treatment for benign paroxysmal positional vertigo secondary to sudden sensorineural hearing loss
por: Li, Gui Fang, et al.
Publicado: (2023)

Fabry disease presenting with sudden hearing loss and otosclerosis: a case report
por: Felisati, Giovanni, et al.
Publicado: (2012)

The Online HEARRING Counselling 1.0 Platform Provides Clinicians with Comprehensive Information on Hearing Device Solutions for Conductive, Mixed, and Sensorineural Hearing Loss
por: Hagen, Rudolf, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_e3du626sdcn0gt2reg0h5uc39g