Vestibular Dysfunction in Turner Syndrome
نویسندگان
چکیده
منابع مشابه
Vestibular dysfunction in Apert Syndrome
Objectives: Apert syndrome affects the craniofacial structures resulting in craniosynostosis, craniofacial anomalies and syndactyly. Although many characteristic features are recognized, vestibular dysfunction is a little known feature that can often be present. This can cause a delay in the attainment of gross motor milestones and impair motor function. We aimed to examine this cohort to revie...
متن کاملTurner syndrome.
Introduction Approximately 1 in 2,500 live female births is affected by Turner syndrome (TS), making it one of the more common genetic conditions encountered in pediatric practice. TS is caused by deletion of all (monosomy) or part (partial monosomy) of the second sex chromosome. Multiple body systems can be affected to varying degrees, presenting both diagnostic and management challenges for t...
متن کاملTurner syndrome
Turner's syndrome is a genetic disorder that affects only females. Turner syndrome is caused by a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. This condition occurs in about 1 out in 2,500 female live births worldwide (but it is much more common among miscarriages and s...
متن کاملvestibular rehabilitation outcomes in the elderly with chronic vestibular dysfunction
background chronic vestibular dysfunction is a frustrating problem in the elderly and can have a tremendous impact on their life, but only a few studies are available. vestibular rehabilitation therapy (vrt) is an important therapeutic option for the neuro-otologist in treating patients with significant balance deficits. objectives the purpose of this study was to assess the effect of vestibula...
متن کاملTurner syndrome
Turner's syndrome is a genetic disorder that affects only females. Turner syndrome is caused by a chromosomal abnormality in which all or part of one of the X chromosomes is missing or altered. While most people have 46 chromosomes, people with TS usually only have 45. This condition occurs in about 1 out in 2,500 female live births worldwide (but it is much more common among miscarriages and s...
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ژورنال
عنوان ژورنال: Otology & Neurotology
سال: 2014
ISSN: 1531-7129
DOI: 10.1097/mao.0b013e31829e16df