Results 81 to 90 of about 73,057 (270)
Rehabilitation with Cochlear Implant in Patient with Harboyan Syndrome
Background Harboyan syndrome, defined as congenital corneal dystrophy associated with progressive sensorineural hearing loss, was first described by Harboyan in 1971.
Lauren Medeiros Paniagua +3 more
doaj +1 more source
Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat +4 more
wiley +1 more source
Characteristics of Mid-Frequency Sensorineural Hearing Loss Progression. [PDF]
OBJECTIVES:To characterize the progression of mid-frequency sensorineural hearing loss (MFSNHL) over time. METHODS:A retrospective chart review spanning 2012 to 2017 was performed at a tertiary care audiology and neurotology center.
Abouzari, Mehdi +9 more
core +2 more sources
Classification and hearing evolution of patients with sudden sensorineural hearing loss [PDF]
The aim of this study was to analyze clinical aspects, hearing evolution and efficacy of clinical treatment of patients with sudden sensorineural hearing loss (SSNHL).
Cruz, Oswaldo Laércio Mendonça +3 more
core +2 more sources
Mitochondrial Syndromic Sensorineural Hearing Loss
Mitochondrial diseases (MD) are a clinically heterogeneous group of disorders that arise as a result of dysfunction of the mitochondrial respiratory chain. Sensorineural hearing loss (SNHL) is often associated to mitochondrial dysfunctions both in syndromic, nonsyndromic forms.
FORLI, FRANCESCA +6 more
openaire +3 more sources
Hereditary sensorineural hearing loss in a bird [PDF]
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
Statistical shape modeling of the human inner ear through micro‐computed tomography imaging
In this study, 54 cadaveric temporal bone specimens underwent high‐resolution micro‐CT imaging. Images were semi‐automatically segmented and converted to 3D surface mesh models for morphological measurement and analysis. Statistical shape models were created for the inner ear, cochlea, and vestibular system, as well as for sex‐ and side‐based subgroups.
Carmine Spedaliere +8 more
wiley +1 more source
Premature infants with hearing loss – A critical review of the literature [PDF]
A stay in the neonatal intensive care unit of greater than 5 days is one of the identified risks of a sensorineural hearing loss. Preterm infants usually have at least one risk factor for hearing impairment.
Rydman, Elin, Uvalic, Gabrijela
core
Introduction Head sense position is coordinated by sensory activity of the vestibular system, located in the inner ear. Children with sensorineural hearing loss may show changes in the vestibular system as a result of injury to the inner ear, which can ...
Renato de Souza Melo +4 more
doaj +1 more source
Delivery strategies of messenger RNA therapeutics for brain disorders
Thus, mRNA therapeutics offer a powerful new avenue for the treatment of brain diseases. This review examines strategies to bypass biological barriers, particularly the blood–brain barrier, and explores emerging delivery systems, such as direct intracerebral injection, intracerebroventricular injection, systemic delivery (including intravenous ...
Kounghwa Youn +5 more
wiley +1 more source

