نتایج جستجو برای: van laere syndrome

تعداد نتایج: 686720  

2018
Sarah Camargos Rita Guerreiro Jose Bras Luis Sergio Mageste

Riboflavin transporter deficiency (formerly known as Brown-Vialetto-Van Laere [BVVL] or Fazio-Londe syndrome) is a neurodegenerative disorder characterized by progressive bulbar palsy with sensorineural deafness or bulbar hereditary neuropathy. It is caused by mutations in the riboflavin transporter genes SLC52A2 (RFVT2) or SLC52A3 (RFVT3). It is a rare syndrome with approximately 70 cases repo...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1991
J M Abarbanel P Ashby A Marquez-Julio K R Chapman

A Caucasian girl developed slowly progressive sensory neural deafness and bulbar and spinal muscle weakness typical of the Vialetto-Van Laere syndrome. As the condition progressed the major disabilities became dysphagia, respiratory muscle weakness and postural hypotension. Treatment with gastrostomy feedings, oxygen and fludrocortisone acetate produced worthwhile functional improvement.

Journal: :Arquivos de neuro-psiquiatria 2007
José Augusto Malheiros Sarah Teixeira Camargos José Teotonio de Oliveira Francisco E C Cardoso

We report the first Brazilian family with Brown-Vialetto-van Laere syndrome. The presence of consanguineous marriages and illness affecting three sisters and one niece support an autosomal recessive transmission. The age at onset of the illness ranged from 12 to 20 years old. The time interval between hearing loss and involvement of other cranial nerves varied from 3 to 12 years. MRI demonstrat...

Journal: :genetics in the 3rd millennium 0
سمیرا یادگاری samira yadegari department of neurology, shariati hospital, tehran university of medical sciences, tehran, iran شهریار نفیسی shahriar nafissi

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 ...

Journal: :Acta neurologica Belgica 2004
Omer Faruk Aydin Dilek Ozçelikel Nesrin Senbil Y K Yavuz Gürer

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...

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1991

2009
Ilse Van der Auwera Cathérine Bovie Cecilia Svensson Xuan B Trinh Ridha Limame Peter van Dam Steven J Van Laere Eric A Van Marck Luc Y Dirix Peter B Vermeulen

Ilse Van der Auwera ([email protected]) Cathérine Bovie ([email protected]) Cecilia Svensson ([email protected]) Xuan B Trinh ([email protected]) Ridha Limame ([email protected]) Peter van Dam ([email protected]) Steven J Van Laere ([email protected]) Eric A Van Marck ([email protected]) Luc Y Dirix ([email protected]) Peter B Vermeulen ...

ژورنال: طب جنوب 2011
سلیمی پور, هومان, نائینی, رزیتا, نفیسی, شهریار, یادگاری, سمیرا,

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...

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