keyword
https://read.qxmd.com/read/38600226/-the-hodokort-trial-and-current-aspects-of-treatment-of-idiopathic-sudden-sensorineural-hearing-loss-with-glucocorticoids
#21
JOURNAL ARTICLE
Stefan K Plontke
No abstract text is available yet for this article.
April 10, 2024: HNO
https://read.qxmd.com/read/38599771/congenital-and-postnatal-cytomegalovirus-case-series-and-state-of-the-science-for-neonatal-providers
#22
REVIEW
Taylor F Salemi, Vanessa R McLean, Amy J Jnah
Cytomegalovirus (CMV), a beta-herpes virus, is the most common viral infection in infants. Transmission may occur congenitally (cCMV) or postnatally (pCMV). Early detection and intervention are crucial in reducing morbidities, notable developmental delays, and sensorineural hearing loss. However, more than 90% of infants are asymptomatic at birth. Treatment involves intravenous ganciclovir or the oral prodrug, valganciclovir, drugs usually reserved for use with symptomatic infants because of the toxicity profile...
April 1, 2024: Neonatal Network: NN
https://read.qxmd.com/read/38599283/japanese-spotted-fever-complicated-by-acute-sensorineural-hearing-loss
#23
Motohiro Shingu, Chieko Fujishima, Shigeo Hara, Hiroaki Nishioka
Japanese spotted fever is an emerging rickettsiosis caused by Rickettsia japonica and is characterized by high fever, rash, and eschar formation. Other symptoms are often vague and nonspecific and include headaches, nausea, vomiting, and myalgia. We present a case of a 46-year-old woman with Japanese spotted fever, complicated by transient bilateral sensorineural hearing loss and presenting cutaneous IgM/IgG immune complex vasculitis. The patient was admitted with a history of several days of high fever, generalized skin erythema, and hearing impairment...
April 8, 2024: Journal of Infection and Chemotherapy: Official Journal of the Japan Society of Chemotherapy
https://read.qxmd.com/read/38595880/cupping-therapy-as-a-potential-complimentary-treatment-for-meniere-s-disease-a-case-report
#24
Tariq S Jamal, Khaled S Aseri, Faisal S Alghamdi, Abdullah M Asiri, Abdulrahman S Hakami
Meniere's disease is defined by the presence of three essential symptoms: episodic vertigo, tinnitus, and sensorineural hearing loss. The mainstay of its management constitutes lifestyle modification and medical and surgical therapies. Cupping therapy is an ancient treatment that is still widely used especially in the Middle East, Africa, and the United Kingdom. This study portraits the case of a 54-year-old patient suffering from long-standing Meniere's disease. The patient was treated with the routine treatment that was to no avail...
March 2024: Curēus
https://read.qxmd.com/read/38595846/a-systematic-review-of-the-clinical-evidence-for-an-association-between-type-i-hypersensitivity-and-inner-ear-disorders
#25
REVIEW
Bin Zeng, Ewa Domarecka, Lingyi Kong, Heidi Olze, Jörg Scheffel, Sherezade Moñino-Romero, Frank Siebenhaar, Agnieszka J Szczepek
Inner ear disorders have a variety of causes, and many factors can contribute to the exacerbation of cochlear and vestibular pathology. This systematic review aimed to analyze clinical data on the coexistence and potential causal interaction between allergic diseases and inner ear conditions. A search of PubMed and Web of Science identified 724 articles, of which 21 were selected for full-text analysis based on inclusion and exclusion criteria. The epidemiologic evidence found overwhelmingly supports an association between allergic disease and particular inner ear disorders represented by a high prevalence of allergic reactions in some patients with Ménière's disease (MD), idiopathic sudden sensorineural hearing loss (ISSHL), and acute low-tone hearing loss (ALHL)...
2024: Frontiers in Neurology
https://read.qxmd.com/read/38593395/clinical-reasoning-a-24-year-old-man-with-gait-impairment-hearing-loss-and-recurrent-fever
#26
JOURNAL ARTICLE
Adriel Rêgo Barbosa, Marianna Pinheiro Moraes de Moraes, Thiago Yoshinaga Tonholo Silva, José Luiz Pedroso, Orlando Graziani Povoas Barsottini
We present a case study of a 24-year-old man who reported mild balance and walking difficulties for 2 years. He had a history of recurrent fever, skin lesions, headache, and elbow pain, but most of these events resolved spontaneously. There was no significant family history. On examination, we observed frontal bossing, sensorineural hearing loss, and gait ataxia. This case underscores the significance of identifying clinical indicators in patients with neurologic symptoms, particularly recurrent fever, to establish a precise and thorough differential diagnosis...
May 14, 2024: Neurology
https://read.qxmd.com/read/38592217/glaucoma-pseudoexfoliation-and-hearing-loss-a-systematic-literature-review
#27
REVIEW
Laura Antonia Meliante, Giulia Piccotti, Lucia Tanga, Sara Giammaria, Gianluca Manni, Giulia Coco
Purpose: To investigate the relationship between glaucoma, pseudoexfoliation and hearing loss (HL). Methods : A systematic literature search following PRISMA guidelines was conducted using the PubMed, Embase, Scopus and Cochrane databases from 1995 up to 28 August 2023. Results : Thirty studies out of the 520 records screened met the inclusion criteria and were included. Most articles (n = 20) analysed the association between pseudoexfoliation syndrome (XFS) and HL, showing XFS patients to have higher prevalence of sensorineural hearing loss (SNHL) at both speech frequencies (0...
February 28, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/38591281/demographic-analysis-of-hearing-impairment-based-on-various-parameters-in-patients-with-cochlear-implant
#28
JOURNAL ARTICLE
Isma Riaz, Amir Rashid, Asifa Majeed
OBJECTIVES: To analyse the demographic and clinical variables in children having undergone cochlear implant surgery because of deafness. METHODS: The cross-sectional study was conducted from January to November 2022 at the Centre for Research in Experimental and Applied Medicine laboratory of the Department of Biochemistry and Molecular Biology, Army Medical College, Rawalpindi, Pakistan, in collaboration with the Ear, Nose and Throat Department of Combined Military Hospital, Rawalpindi, and comprised children of eith gender aged up to 10 years who had received cochlear implant...
March 2024: JPMA. the Journal of the Pakistan Medical Association
https://read.qxmd.com/read/38590173/case-report-antibiotic-irrigation-and-drainage-tube-for-managing-chronic-suppurative-otitis-media-after-cochlear-implantation
#29
JOURNAL ARTICLE
Jiaying Li, Ningyu Wang, Juan Zhang
Cochlear implantation (CI) is the most effective solution for patients with severe-to-profound sensorineural hearing loss, especially in children. However, a major postoperative complication, known as chronic suppurative otitis media (CSOM), poses challenges for both doctors and families of the patients, which can affect post-CI hearing outcomes. We present the case of post-CI CSOM in a 15-year-old girl. She had been utilizing a unilateral cochlear implant for 7 years and had been experiencing intermittent earache and discharge in her only audible ear for the past 15 months...
April 8, 2024: Ear, Nose, & Throat Journal
https://read.qxmd.com/read/38586037/impact-of-reduced-spectral-resolution-on-temporal-coherence-based-source-segregation
#30
Vibha Viswanathan, Michael G Heinz, Barbara G Shinn-Cunningham
Hearing-impaired listeners struggle to understand speech in noise, even when using cochlear implants (CIs) or hearing aids. Successful listening in noisy environments depends on the brain's ability to organize a mixture of sound sources into distinct perceptual streams (i.e., source segregation). In normal-hearing listeners, temporal coherence of sound fluctuations across frequency channels supports this process by promoting grouping of elements belonging to a single acoustic source. We hypothesized that reduced spectral resolution-a hallmark of both electric/CI (from current spread) and acoustic (from broadened tuning) hearing with sensorineural hearing loss-degrades segregation based on temporal coherence...
March 13, 2024: bioRxiv
https://read.qxmd.com/read/38585549/a-homozygous-missense-variant-in-hsd17b4-identified-in-two-different-families
#31
JOURNAL ARTICLE
Pınar Özkan Kart, Yavuz Sahin, Nihal Yildiz, Alper Han Cebi, Gulnur Esenulku, Ali Cansu
BACKGROUND: Perrault syndrome is an inherited disorder with clinical findings that differ according to sex. It is characterized by a variable age of onset and sensorineural hearing loss in both sexes, as well as ovarian dysfunction in females with a 46,XX karyotype. Although it is a rare autosomal recessive syndrome, with approximately 100 affected individuals reported in the literature, it shows both genotypic and phenotypic variations. Mutations in the HSD17B4 gene have been identified as one of the genetic causes of Perrault syndrome...
March 2024: Molecular Syndromology
https://read.qxmd.com/read/38584364/photografted-zwitterionic-hydrogel-coating-durability-for-reduced-foreign-body-response-to-cochlear-implants
#32
JOURNAL ARTICLE
Adreann Peel, Douglas Bennion, Ryan Horne, Marlan R Hansen, C Allan Guymon
The durability of photografted zwitterionic hydrogel coatings on cochlear implant biomaterials was examined to determine the viability of these antifouling surfaces during insertion and long-term implant usage. Tribometry was used to determine the effect of zwitterionic coatings on the lubricity of surfaces with varying hydration levels, applied normal force, and time frame. Additionally, flexural resistance was investigated using mandrel bending. Ex vivo durability was assessed by determining the coefficient of friction between tissues and treated surfaces...
April 7, 2024: ACS Applied Bio Materials
https://read.qxmd.com/read/38583982/high-frequency-hearing-vulnerability-associated-with-the-different-supporting-potential-of-hensen-s-cells-smart-seq2-rna-sequencing
#33
JOURNAL ARTICLE
Yiding Yu, Yue Li, Cheng Wen, Fengbo Yang, Xuemin Chen, Wenqi Yi, Lin Deng, Xiaohua Cheng, Ning Yu, Lihui Huang
Hearing loss is the third most prevalent physical condition affecting communication, well-being, and healthcare costs. Sensorineural hearing loss often occurs first in the high-frequency region (basal turn), then towards the low-frequency region (apical turn). However, the mechanism is still unclear. Supporting cells play a critical role in the maintenance of normal cochlear function. The function and supporting capacity of these cells may be different from different frequency regions. Hensen's cells are one of the unique supporting cell types characterized by lipid droplets (LDs) in the cytoplasm...
April 5, 2024: Bioscience Trends
https://read.qxmd.com/read/38581347/papulo-vesicular-eruption-and-profound-unilateral-hearing-loss-in-a-20-year-old-man
#34
Henning Klapproth, Jonas Rauterberg, Sami Shabli, Steffi Silling, Sindy Böttcher, Esther von Stebut, Mario Fabri
No abstract text is available yet for this article.
April 6, 2024: Journal der Deutschen Dermatologischen Gesellschaft: JDDG
https://read.qxmd.com/read/38576930/alstrom-syndrome-with-classical-findings-a-rare-case-report-of-monogenic-ciliopathy-co-occurrence-in-twins
#35
Sagun Ghimire, Suman Simkhada, Samir Thapa, Kiran Ghising
INTRODUCTION AND IMPORTANCE: Alstrom syndrome is one of the rarest monogenic ciliopathy belonging to autosomal recessive disorder. The pathophysiology of Alstrom syndrome is not well understood but based upon the available medical literature its mechanism can be linked with recessive mutation in Alstrom syndrome 1(ALSM1) gene resulting in various multiple organ involvement and poor prognosis. Moreover the co-occurrence of such syndrome simultaneously in twins in same period of time is considered rare...
April 2024: Annals of Medicine and Surgery
https://read.qxmd.com/read/38576800/effect-of-foot-reflexology-on-an-infant-with-sensorineural-hearing-loss-a-case-report
#36
Yu-Jun Lee, Mao-Qing Chen, Jie Dong
BACKGROUND: Our study contributes to the further understanding of the mechanism of foot reflexology. Foot reflexology has been reported to affect hearing recovery, but no physiological evidence has been provided. This lack of evidence hampers the acceptance of the technique in clinical practice. CASE SUMMARY: A girl was taken to North Sichuan Medical University Affiliated Hospital for a hearing screen by her parents. Her parents reported that her hearing level was the same as when she was born...
March 16, 2024: World Journal of Clinical Cases
https://read.qxmd.com/read/38574210/newborn-skin-part-i-common-rashes-and-skin-changes
#37
JOURNAL ARTICLE
Katherine A M Snyder, Adam D Voelckers
Rashes in the newborn period are common and most are benign. Infections should be suspected in newborns with pustules or vesicles, especially in those who are not well-appearing or have risk factors for congenital infection. Congenital cytomegalovirus infection can cause sensorineural hearing loss and neurodevelopmental delay. Skin manifestations of cytomegalovirus may include petechiae due to thrombocytopenia. The most common skin manifestations of early congenital syphilis are small, copper-red, maculopapular lesions located primarily on the hands and feet that peel and crust over three weeks...
March 2024: American Family Physician
https://read.qxmd.com/read/38571700/children-with-non-central-nervous-system-tumors-treated-with-platinum-based-chemotherapy-are-at-risk-for-hearing-loss-and-cognitive-impairments
#38
JOURNAL ARTICLE
Allison J L'Hotta, Anne Spence, Taniya E Varughese, Kara Felts, Susan S Hayashi, Megan Jones-White, Emily LaFentres, Judith E C Lieu, Robert J Hayashi, Allison A King
BACKGROUND: Childhood cancer survivors (CCS) with chemotherapy induced sensorineural hearing loss (SNHL) are at risk for neurocognitive impairments. The purpose of this study was to determine the relationship between SNHL and cognitive function among CCS. PROCEDURE: Inclusion: non-CNS solid tumor diagnosis; history of platinum chemotherapy (cisplatin and/or carboplatin); 8-17 years of age; off anti-cancer treatment for ≥6 months; and English speaking. Exclusion: history of intrathecal chemotherapy, cranial radiation, or baseline neurocognitive disorder...
2024: Frontiers in Pediatrics
https://read.qxmd.com/read/38569205/a-case-of-alstr%C3%A3-m-syndrome-with-a-novel-variant-in-alms1-gene-presenting-with-cone-rod-dystrophy-as-first-finding
#39
JOURNAL ARTICLE
Busra Yen, Mukaddes Damla Ciftci, Filiz Afrashi, Huseyin Onay, Damla Goksen
PURPOSE: Alström Syndrome (AS) is a rare autosomal recessive monogenic ciliopathy which is caused by a mutation of the Alström syndrome 1 (ALMS1) gene. It is a multisystemic disorder characterized by insulin resistance, childhood obesity, cardiomyopathy, progressive hepatic and renal failure, sensorineural hearing loss and retinal degeneration. Herein, we aimed to report a novel variant in ALMS1 gene causing AS in a patient presenting with visual impairment. METHODS: Case report...
April 1, 2024: Retinal Cases & Brief Reports
https://read.qxmd.com/read/38567212/pediatric-cochlear-implants-in-the-chudley-mccullough-syndrome-a-report-of-two-cases
#40
Noah E Alter, Kailey Introcaso, Cathy Nunez, Leonor Roach, Samuel T Ostrower
Chudley-McCullough syndrome (CMS) is a rare autosomal recessive disorder characterized by sensorineural hearing loss and cerebral abnormalities, including ventriculomegaly and partial dysgenesis of the corpus callosum. CMS is caused by two inactivating mutations of the G protein signaling modulator 2 (GPSM2), which maintains inner hair cell polarity and spindle orientation. Since its initial description, CMS has been reported approximately 30 times in the medical literature with several individuals undergoing cochlear implantation to restore their hearing...
March 2024: Curēus
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