نتایج جستجو برای: congenital hearing loss
تعداد نتایج: 597503 فیلتر نتایج به سال:
Pendard syndrome is a genetic disorder that is usually associated with hearing loss in children and thyroid status called goiter, and sometimes affects the balance of the person. Researchers estimate that 7 to 8 percent of the total congenital hearing loss is Pandard's syndrome. A sign that a person may have mutated the SLC26A4 gene is a family history of hearing loss in the early days. Another...
Introduction: Semicircular canal dehiscence (SCD) syndrome has been defined as a bone defect in the roof of the superior, posterior and lateral semicircular canals. We reported that three-dimension CT and MR imaging of superior SCD is rare in english literature. Case presentation: A 6-year-old boy patient presented with hearing loss and left facial nerve paresis since birth. CT and MR images de...
ipsilateral absence of tonsil and microtia with ectopic salivary gland was reported by Sinha & Singh in 1978.This patient presented with left external ear deformity with conductive hearing loss His oropharyngeal examination found ipsilateral absence of tonsil and ectopic salivary gland in the posterior part of the tongue. In 1985 Grewal, Hiranandini and Kalgutkar reported 4 cases of congenital ...
The incidence of sensorineural hearing loss among infants in the neonatal intensive unit (NICU) is higher than in normal infants. This study determined the rate of hearing loss in healthy newborns and in NICU patients before hospital discharge at a single institution in the Eastern region of the United Arab Emirates; 96.5% of all eligible infants were screened. Hearing deficit was diagnosed in ...
BACKGROUND The natural history of congenital cytomegalovirus (CMV) infection is scarcely known in populations with high maternal CMV seroprevalence. This study evaluated the birth prevalence, clinical findings at birth, and hearing outcome in CMV-infected children from such a population. METHODS Consecutively born infants were screened for the presence of CMV in urine and/or saliva specimens ...
Introduction Congenital cholesteatomas of the temporal bone are epidermoid cysts of embryologic origin that result in progressive desquamation and trapping of squamous epithelium behind an intact tympanic membrane. They are benign, slowly progressive lesions that can be found in various areas of the temporal bone. We report a case of a patient with a massive cholesteatoma first detected at the ...
Early hearing deprivation could affect the development of auditory, language, and vision ability. Insufficient or no stimulation of the auditory cortex during the sensitive periods of plasticity could affect the function of hearing, language, and vision development. Twenty-three infants with congenital severe sensorineural hearing loss (CSSHL) and 17 age and sex matched normal hearing subjects ...
Congenital or acquired hearing loss in infants and children has been linked with lifelong deficits in speech and language acquisition, poor academic performance, personal-social maladjustments, and emotional difficulties. Identification of hearing loss through neonatal hearing screening, regular surveillance of developmental milestones, auditory skills, parental concerns, and middle-ear status ...
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