نتایج جستجو برای: dyt6 dystonia

تعداد نتایج: 6616  

Journal: : 2021

One of the important areas modern neurology is movement disorders, due to their negative impact on daily activity and quality life patients. Dystonia third most common extrapyramidal disease. Often, dystonia accompanied by trembling hyperkinesis, however, known data dystonic tremor are scattered not systematized, its fixation causes difficulties lack clear tremorographic characteristics. Many i...

2012
Yoshimichi Miyazaki Wataru Sako Kotaro Asanuma Yuishin Izumi Tetsuro Miki Ryuji Kaji

Although there are some newly developed options to treat dystonia, its medical treatment is not always satisfactory. Zolpidem, an imidazopyridine agonist with a high affinity on benzodiazepine subtype receptor BZ1 (ω1), was found to improve clinical symptoms of dystonia in a limited number of case reports. To investigate what subtype of dystonia is responsive to the therapy, we conducted an ope...

Journal: :Expert review of neurotherapeutics 2006
Roongroj Bhidayasiri Daniel Tarsy

Dystonia may be a sign or symptom, that is comprised of complex abnormal and dynamic movements of different etiologies. A specific cause is identified in approximately 28% of patients, which only occasionally results in specific treatment. In most cases, treatment is symptomatic and designed to relieve involuntary movements, improve posture and function and reduce associated pain. Therapeutic o...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2002
Carolyn E Pizoli H A Jinnah Melvin L Billingsley Ellen J Hess

Dystonia is a relatively common neurological syndrome characterized by twisting movements or sustained abnormal postures. Although the basal ganglia have been implicated in the expression of dystonia, recent evidence suggests that abnormal cerebellar function is also involved. In these studies, a novel mouse model was developed to study the role of the cerebellum in dystonia. Microinjection of ...

Journal: :Brain : a journal of neurology 2009
Fabienne Clot David Grabli Cécile Cazeneuve Emmanuel Roze Pierre Castelnau Brigitte Chabrol Pierre Landrieu Karine Nguyen Gérard Ponsot Myriem Abada Diane Doummar Philippe Damier Roger Gil Stéphane Thobois Alana J Ward Michael Hutchinson Annick Toutain Fabienne Picard Agnès Camuzat Estelle Fedirko Chankannira Sân Delphine Bouteiller Eric LeGuern Alexandra Durr Marie Vidailhet Alexis Brice

Dopa-responsive dystonia is a childhood-onset dystonic disorder, characterized by a dramatic response to low dose of L-Dopa. Dopa-responsive dystonia is mostly caused by autosomal dominant mutations in the GCH1 gene (GTP cyclohydrolase1) and more rarely by autosomal recessive mutations in the TH (tyrosine hydroxylase) or SPR (sepiapterin reductase) genes. In addition, mutations in the PARK2 gen...

Journal: :Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2011
Nutan Sharma Ramon A Franco

Spasmodic dysphonia, a form of the neurologic condition known as dystonia, results from involuntary spasms of the larynx, producing interruptions of speech and changes in voice quality. The pathogenesis of spasmodic dysphonia is not well understood. However, several genetic mutations have been identified that cause different forms of dystonia. In some individuals, these genetic mutations result...

Journal: :Pain 2007
Monique A van Rijn Johan Marinus Hein Putter Jacobus J van Hilten

Complex regional pain syndrome (CRPS) may lead to movement disorders (MDs) in some patients. Reliable information on the nature, chronology and clinical determinants of MDs in CRPS patients is lacking but could provide better insight in to the underlying pathophysiological mechanism. We retrospectively evaluated the clinical and temporal characteristics of MDs in patients with CRPS. Cox's propo...

Journal: :Journal of neurology, neurosurgery, and psychiatry 1984
C D Marsden M H Marion N Quinn

Twenty-three children (aged less than 18 years) and 17 adults with severe widespread dystonia were treated with high doses of benzhexol (up to 130 mg daily introduced slowly over many weeks). Children tolerated higher doses (median 30 mg/day) than adults (median 20 mg/day). 52% of the children gained useful benefit, many (43%) without unwanted side effects. Such an approach was less successful ...

Journal: :Neurology 2006
A Schmidt H-C Jabusch E Altenmüller J Hagenah N Brüggemann K Hedrich R Saunders-Pullman S B Bressman P L Kramer C Klein

Musician's dystonia is generally considered a sporadic disorder. We present three families with the index patient affected by musician's dystonia, but other forms of upper limb focal task-specific dystonia (FTSD), mainly writer's cramp, in seven relatives. Our results suggest a genetic contribution to FTSD with phenotypic variability, including musician's dystonia.

Journal: :The American journal of psychiatry 1993
P Sachdev

Clinical characteristics of 15 consecutively referred patients with tardive dystonia are reported. The onset of tardive dystonia occurred in all age groups and in both sexes, with some preponderance in men. There was considerable overlap with tardive dyskinesia and tardive akathisia. Six subjects reported past acute dystonia, and four had histories of essential tremor, suggesting a vulnerabilit...

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