Results 31 to 40 of about 42,754 (253)

Sensorineural hearing loss and prematurity [PDF]

open access: yesArchives of Disease in Childhood - Fetal and Neonatal Edition, 2000
OBJECTIVE To elucidate clinical antecedents of sensorineural hearing loss (SNHL) in very preterm infants. DESIGN Case-control study. SUBJECTS Fifteen children < 33 weeks ...
E S, Marlow, L P, Hunt, N, Marlow
openaire   +2 more sources

Bilateral Sudden Sensorineural Hearing Loss after Treatment of Aneurysmal Subarachnoid Hemorrhage by Angiographic Embolization: A Case Report

open access: yesTurkish Archives of Otorhinolaryngology, 2014
Bilateral sudden sensorineural hearing loss is a rare otologic emergency and constitutes 0.44%-4.9% of overall sudden sensorineural hearing loss cases. Microvascular dysfunction secondary to systemic cardiovascular diseases, such as embolism, vasospasm ...
Çağatay Han Ülkü, Abitter Yücel
doaj   +1 more source

Sudden sensorineural hearing loss (SSHL) following a local anesthetic dental procedure

open access: yesJournal of Otology, 2019
Acute sensorineural hearing loss is an uncommon phenomenon in dentistry. We describe the case of a 79-year-old male who presented with acute sensorineural hearing loss occurring 2 days after a tooth extraction procedure under local anesthesia.
Yi Wang   +5 more
doaj   +1 more source

Sensorineural hearing loss in neurobrucellosis

open access: yesNeurosciences, 2008
Neurobrucellosis (NB) is a rare clinical presentation of brucellosis. This form is hard to diagnose because of a lack of definite diagnostic criteria, and its treatment is also hard. The clinical spectrum may cover a span between non-specific neurological symptoms to a severe meningoencephalitis.
Gonul, Sengoz   +3 more
openaire   +2 more sources

Hereditary sensorineural hearing loss in a bird [PDF]

open access: yesNaturwissenschaften, 1994
The avian cochlea is the principal model for the investigation of hair-cell regeneration and the recovery of function in the vertebrate auditory periphery [1]. This capacity for repair in birds would seem to preclude permanent sensorineural hearing loss involving hair cells, which is the most common cause of hearing disabilities in humans [2]. Here, we
Gleich, Otto   +2 more
openaire   +3 more sources

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi   +2 more
wiley   +1 more source

Convalescence of auditory brainstem response following idiopathic sudden onset sensorineural hearing loss

open access: yesPediatria i Medycyna Rodzinna, 2018
Sudden onset sensorineural hearing loss is an emergency condition in otorhinolaryngology. Despite its common occurrence, the investigation and treatment of this condition are still controversial. Auditory brainstem response is one of hearing assessment
Khairunnisak Misron   +2 more
doaj   +1 more source

Audiological findings of a patient with H syndrome: case report

open access: yesThe Egyptian Journal of Otolaryngology, 2021
Background H syndrome is an autosomal recessive disorder caused by mutations in SLC29A3. Hyperpigmentation, hypertrichosis, hyperglycemia, and hearing loss are some characteristics of this disorder, and it has a prevalence of
Diala Hussein   +2 more
doaj   +1 more source

Developmental and Epileptic Encephalopathy due to Biallelic Pathogenic Variants in PIGM

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective PIGM encodes a critical enzyme in the glycosylphosphatidylinositol (GPI)‐anchor biosynthesis pathway. While promoter‐region mutations in PIGM have been associated with a relatively mild phenotype characterized by portal vein thrombosis and absence seizures, recent evidence suggests that coding‐region mutations result in a more severe
Júlia Sala‐Coromina   +11 more
wiley   +1 more source

Endothelial Cell Proteins as Biomarkers in Susac Syndrome

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Susac syndrome (SS) is a rare CD8+ T cell–mediated microangiopathy affecting the brain, retina, and auditory labyrinth. Endothelial injury is thought to be a central mechanism; however, no circulating disease biomarkers are known. We performed targeted proteomic profiling to identify circulating endothelial‐associated proteins as ...
Rohit Benjamin   +11 more
wiley   +1 more source

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