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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Visual symptoms are common in autosomal recessive cerebellar ataxias but the responses to therapy are generally poor.

Schalling E, Hartelius L. There are no specific or curative treatments for XLCA and the optimal management is directed to provide better quality of life with comprehensive rehabilitation program, including interdisciplinary care such as occupational and physical therapy, for behavioral and cognitive impairment and motor incoordination.

Although these findings may indicate potential effectiveness, experience of many ataxic clinics is less promising Alpha lipoic acid can facilitate glucose transport and has been proposed to treat Glut1 deficiency As a result, riluzole may reduce neuronal hyperexcitability. Miglustat consistently improved swallowing functions in NPC patients in multiple studies LDL apheresis was also effective in reducing the cholestanol levels without dramatic effects in ataxic symptoms Parkinsonism suggesting nigrostriatal dysfunction should be treated with levodopa.

Hereditary ataxias HA represents an extensive group of clinically and genetically heterogeneous neurodegenerative diseases, characterized by progressive ataxia combined with extra-cerebellar and multi-systemic involvements, including peripheral neuropathy, pyramidal signs, movement disorders, seizures, and cognitive dysfunction.

Sleep ataia in cerebellar ataxias.

Current concepts in the treatment of hereditary ataxias

HA are divided by different inheritance patterns, such as, autosomal recessive, autosomal dominant, X-linked, and mitochondrial ataxias 1. Ataxia associated with CoQ10 deficiency can be divided into primary and secondary CoQ10 deficiency. Dystonia and head tremor are the common clinical features for AVED 5. Propranolol and primidone should be tried in patients with postural and action tremor.

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Several different drugs have been reported to improve symptoms of EA1 and EA2. It has been shown to prevent pathological aggregation of proteins within cells in several diseases associated with abnormal cellular-protein aggregation. X-linked disorders with cerebellar dysgenesis. Experimental data indicates cerebslar inhibition of histone deacetylase corrects this pathological heterochromatinisation and leads to increased expression of frataxin FXN No warranty is given about the accuracy of the copy.

Non-neurological symptoms could also impact the quality of life in patients with autosomal recessive cerebellar ataxias and proper treatment is also important. Speech therapy may benefit patients with dysarthria and dysphagia These disorders are relatively rare and large-scaled randomized, controlled clinical trials are usually not available. A randomized double-blind study evaluated the effect and safety of oral zinc 50mg supplementation for 36 patients with SCA2.

Another study cerebelwr the effect of inpatient rehabilitation of patient with FRDA. Pain is more frequent musculoskeletal, but in a smaller subset may be related to dystonia or neuropathy. Nonetheless, successful treated cases can provide guidelines to manage these rare disorders.

Motor training in degenerative spinocerebellar disease: Varenicline was also studied. Table 1 describes the main current symptomatic treatment proposed for autosomal recessive cerebellar ataxia. A previous cohort study with patients described worse quality of life in patients with depressive symptoms.

Treatment of the underlying metabolic abnormality in autosomal recessive ataxias could cereblear lead to stabilization or improvement of ataxic symptoms. Furthermore, neurologists must bear in mind that some types of hereditary ataxias such as vitamin E and CoQ10 deficiency are treatable.

Primary and secondary ataxias. Non-neurological symptoms Non-neurological symptoms could also impact the quality of life in patients with autosomal recessive cerebellar ataxias and proper treatment is also important.

We concluded that with the inhibition of this wave, there was a decrease in the anxiety, promoting a muscle relaxing and better equilibrium. Rehabilitation therapy is not well studied in hereditary ataxias. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Miglustat is a glucosylceramide synthase inhibitor that reduces the accumulating glycolipids 8. Regarding ataxias, no curative treatment has emerged, but there are clinical studies currently underway using this kind of approaches. Hereditary ataxias HA represents an extensive group of clinically and genetically heterogeneous neurodegenerative diseases, characterized by progressive ataxia combined with extra-cerebellar and multi-systemic involvements, including peripheral neuropathy, pyramidal signs, movement disorders, seizures, and cognitive dysfunction 1.

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Miglustat was recommended to treat dystonic symptoms in CTX Tratxmento dominant cerebellar ataxias There are a few randomized trials for symptoms treatment in autosomal dominant ataxias. On the other hand, there is insufficient information for speech therapy. A randomized, phase 2 clinical trial of lithium carbonate in Machado-Joseph disease. Muscle cramp in Machado-Joseph disease: Views cerebela Reviews Current concepts in the treatment of hereditary ataxias.

Other neurological symptoms Visual symptoms are common ataxix autosomal recessive cerebellar ataxias but the responses to therapy are generally poor. Recently, Romano et al. Symptomatic treatment for pain, cramps and spasticity are not well studied in patients with SCA. Some phase I clinical trials using these targeted therapies have been already completed mostly for FRDA and others are about to begin.

Coenzyme Q 10 -responsive ataxia: Nevertheless, speech therapy should go beyond assessment.