ATAXIA CEREBELAR TRATAMENTO PDF

ATAXIA CEREBELAR TRATAMENTO PDF

Title: Equilíbrio estático por baropodometria em paciente com ataxia cerebelar após tratamento com neurofeedback. (Portuguese); Alternate Title: Static balance . ataxia cerebelar tratamento pdf idiopathic late onset cerebellar ataxia have no affected relatives and will normally be given a low risk of passing on the disease . utilizadas em ensaios clínicos para tratamento da FRDA, porém sua eficácia ainda é . de SC em vérmis e hemisférios cerebelares e atrofia de SB cerebelar .

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Current concepts in the treatment of hereditary ataxias

Teive HA, Ashizawa T. Physical therapy may lead to improvement in ataxia symptoms and ataixa life functions; occupational therapy may improve global function status and diminish symptoms of depression. Other drugs should be tried: Ceeebelar for Machado-Joseph disease: Psychiatric symptoms are very common in SCA. In addition, techniques capable of interfering with gene expression are now available, such as RNA interference, oligo antisense nucleotides, gene fratamento and epigenetic-based therapy.

Epilepsy is very common in Glut1 deficiency syndrome and diet modifications are highly effective in either reducing or even eliminating the seizures in these patients Intensive rehabilitation therapy combining physical therapy and occupational may provide the best results Neurofeedback is a device that can detect brain wave patterns and redirect them to optimize balance and brain potentials and has been used in recent years in athletes and neurological conditions.

Convenzione di vienna 69 pdf

Sleep disorders have already been recognized as one of the most important non-motor manifestations in SCAs. Table 3 describes the main rehabilitation strategies in hereditary ataxias.

Spinocerebellar ataxias caused by polyglutamine expansions: In this group of HA we can add two other forms of ataxia: In this review, we will focus on the symptomatic treatment of the main autosomal recessive ataxias, autosomal dominant ataxias, X-linked cerebellar ataxias and mitochondrial ataxias. These patients may have chronic daily pain, specially evolving back and legs These disorders cerbeelar relatively rare and large-scaled randomized, controlled clinical trials are usually not available.

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The autosomal recessive cerebellar ataxias. Therefore, several mechanism-based therapies are available to correct the underlying defective metabolic pathways. Muzar Z, Lozano R. Experimental data indicates that inhibition of histone deacetylase corrects this pathological heterochromatinisation and leads to increased expression of frataxin FXN There are a few randomized trials for symptoms treatment in autosomal dominant ataxias.

Services on Demand Journal. Some patients with SCA3 may have a levodopa-responsive-Parkinsonism 31 University of Washington, Cerebrlar [cited Nov 17]. Improvement of pain may be obtained with usual doses of baclofen, cyclobenzaprine and amitriptyline.

The cetebelar features of XLCA include hypotonia, developmental ataxai, intellectual impairment and ataxia GLUT1 deficiency and other glucose transporter diseases. The role for symptomatic treatment on autosomal dominant ataxias is divided into the following symptoms: Propranolol and primidone should be tried in patients with postural and action tremor. Other ataaxia disorders Movement disorders are quite common in SCAs and may be a prominent symptom.

Vitamin supplementation can improve the growth rate in the pediatric patients with abetaliproproteinemia. A combination of CDCA and statins have been proposed, which effectively normalized the blood bile acid biochemistry but did not improve cerebellar ataxia Ataxia is a disorder of balance and coordination and may be classified in different forms 1.

A previous cohort study with patients described worse quality of life in patients with depressive symptoms. Speech therapy may benefit patients with dysarthria and dysphagia Sleep disorders Sleep disorders have already been recognized as one of the most important non-motor manifestations in SCAs.

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Convenzione di vienna 69 pdf

Mitochondrial diseases are clinically heterogeneous disorders resulted from dysfunction of the mitochondrial respiratory chain, which is the final common pathway for aerobic metabolism. Miglustat was recommended to treat dystonic symptoms in CTX Plasma phytanic acid levels and clinical symptoms might improve only after several month of diet modification We concluded that with the inhibition of this wave, there was a decrease in the anxiety, promoting a muscle relaxing and better equilibrium.

Botulinum toxin injection may be used in focal or segmental cases of dystonia Other putative biomarkers must be identified and validated to speed up the therapeutic trials for ataxias. Secondary CoQ10 deficiency is associated with other genetic mutations such as aprataxin and mitochondrial genes Other neurological symptoms Visual symptoms are common in autosomal recessive cerebellar ataxias but the responses to therapy are generally poor.

There is no conflict of interest to declare.

More recently, another approach for SCA patients have been studied using leg cycling therapy. As a result, tissues that are highly dependent on aerobic metabolism are preferentially involved in mitochondrial tratamsnto. Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by CAG n repeat detection. Botulinum toxin injection may improve spasticity in patients with SCAs Dystonia and head tremor are the common clinical features for AVED 5.

As a result, riluzole may reduce neuronal hyperexcitability. The effectiveness of allied health care in patients with ataxia: Autosomal dominant cerebellar ataxias are divided in two main groups: