brown-vialetto-van laere syndrome: report of five iranian cases
نویسندگان
چکیده
brown-vialetto-van laere syndrome (bvvls) is a rare neurological disorder of unknown etiology considered to be a form of motor neuron diseases. this syndrome is characterized by bilateral deafness and involvement of lower cranial nerves, especially 7th-12th. umn signs are less frequent. until 2007, only fifty eight cases were reported. half of the reported cases were sporadic. in the remaining cases, different patterns of inheritance were suggested including autosomal recessive, autosomal dominant and x-linked. we describe 5 cases of bvvls (4 females and 1 male) who were all sporadic, with a history of parents consanguinity in 2 of them. our study is the first case report from iran and one of the largest series ever reported and emphasizes the necessity to investigate the molecular pathogenesis of this syndrome.
منابع مشابه
Brown-Vialetto-Van Laere syndrome
The Brown-Vialetto-Van Laere syndrome (BVVL) is a rare neurological disorder characterized by progressive pontobulbar palsy associated with sensorineural deafness. Fifty-eight cases have been reported in just over 100 years. The female to male ratio is approximately 3:1. The age of onset of the initial symptom varies from infancy to the third decade. The syndrome most frequently presents with s...
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We describe a 14-year-old female patient with progressive ponto-bulbar palsy and deafness. The first symptom was present at the age of 9 as a difficulty in walking and then she was stable with mild clumsy walking till 14 year-old. It was noticed that she had rapidly progression gait disorder, hearing loss, difficulty in swallowing and speaking in a period of 2.5 months. Clinically, there were b...
متن کاملFour cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings
Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare neurological disorder. We report our finding about four patients clinically and electrophysiologically diagnosed as BVVLS and denoted their clinical features with comparison to previous reports. The first symptom was bilateral hearing loss and the onset of other cranial nerves involvement varied between 0-15 years. Our patients represented som...
متن کاملمروری برسندرم Brown-Vialetto-Van Laere و تشخیصهای افتراقی آن
زمینه: سندرم Brown-Vialetto-Van Laere یکی از بیماریهای تحلیل برنده نورولوژیک است که جزء اختلالات نورون حرکتی طبقهبندی میشود. این سندرم بهلحاظ اپیدمیولوژیک نادر بوده اما در مناطق مختلف دنیا گزارش شده است. تظاهر بیماری اغلب بهصورت کاهش شنوایی دوطرفه و فلج پیشرونده پونتوبولبر است. درگیری بخش موتور اعصاب کرانیال تحتانی نیز دیده میشود. تشخیص بر اساس یافتههای بالینی و الکتروفیزیولوژی و رد نمود...
متن کاملfour cases of brown-vialetto-van laere syndrome from iran: clinical and electrophysiologic findings.
brown-vialetto-van laere syndrome (bvvls) is a rare neurological disorder. we report our finding about four patients clinically and electrophysiologically diagnosed as bvvls and denoted their clinical features with comparison to previous reports. the first symptom was bilateral hearing loss and the onset of other cranial nerves involvement varied between 0-15 years. our patients represented som...
متن کاملAssociation of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS.
UNLABELLED Genetic variants in UBQLN1 gene have been linked to neurodegeneration and mutations in UBQLN2 have recently been identified as a rare cause of amyotrophic lateral sclerosis (ALS). OBJECTIVE To test if genetic variants in UBQLN1 are involved in ALS. METHODS 102 and 94 unrelated patients with familial and sporadic forms of ALS were screened for UBQLN1 gene mutations. Single nucleot...
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عنوان ژورنال:
genetics in the 3rd millenniumجلد ۷، شماره ۳، صفحات ۱۷۷۶-۱۷۷۶
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