One liter of tears: "Spinocerebellar degeneration", explains

You have Spinocerebellar degeneration? It is also known as Spinocerebellar irregularity. I really have no idea about this disease until I saw "1 liter of tears" as "A liter no Namida" or "A diary with tears" or "A Diary of Tears". It is a Japanese TV drama series, an adaptation of a Japanese girl named Aya Kito diary. This drama series is one of the best TV series I have ever seen. You feel the pain feels your family actually. Ikeuchi Aya was played by Erika Sawajiri the girl who suffers Spinocerebellar degeneration. The drama is so touching heart, the entire series will make everyone to see.Now I'll change the topic and give you some information about this disease. Sorry to say but this disease is not curable. I want this on my blog to share it all, no idea which not written about this disease. We help each other to share information like this so that everyone will be aware of. I can only pain how, what, happened to the girl take. So hard to see someone who always into the ground and getting hurt this was because a person suffering from actually have problems in controlling ling your muscles. Spinocerebellar ataxia (SCA): a progressive, degenerative, genetic disease each a disease in its own right could be considered with multiple types. Symptoms:Spinocerebellar ataxia is a group of inherited disorders characterized by slowly progressive balance disorders of gait often associated with poor coordination of hands, speech and eye movements. Often occurs atrophy of the cerebellum and various Ataxias are known to affect different regions within the Kleinhirns.Wie other forms of, a failure of the fine tuning of muscle movements does body movement SCA unsure and awkward together with other Symptomen.Die symptoms of ataxia vary ataxia with the specific type and the individual patient. Generally a person with ataxia retains full intellectual capacity, but it can gradually lose physical control.Treatment and prognosis:There is no known cure for ataxia irregularity, a progressive disease (it gets worse with time), although not all types cause equally severe disability.Treatments are generally on the softening symptoms, not the disease itself is limited. The condition may be irreversible. A person with this condition is usually end, who must use a wheelchair, and finally you may need help to perform daily tasks.Treatment of loss of balance or ataxia, then includes mostly using adaptive devices allow ataxic each to maintain as much independence as possible. Such devices may include a stick, crutches, Walker or wheelchair for those with impaired gait; With writing devices, supporting feeding and self-care when hand and poor coordination are impaired; and communication devices for those with impaired Rede.Viele have other symptoms besides ataxia patients with hereditary or idiopathic forms of ataxia. Drugs or other therapies may be for some of these symptoms suitable that could include, tremor, rigidity, depression, spasticity and sleep disorders, among other things.Both experience the first symptoms and duration of the disease can be subject to fluctuations. If the disease by expansion in Polyglutamine Trinucleotide will cause repetition CAG, can result in a longer expansion to an earlier onset and a more radical progression of clinical symptoms.Diagnosis:It can easily be diagnosed as another neurological disorder such as multiple sclerosis (MS).The most precise means of identifying of SCA, including the special kind is by DNA analysis. Asymptomatic and risk should consult given a genetic test to a doctor and the genetic counselor family members. An MRI of the brain can also show whether certain regions of cerebellum have significantly deteriorate but this is often not the most stable way to make a diagnosis.SCA is related with Olivopontocerebellar atrophy (OPCA); SCA are 1, 2 and 7 types of OPCA. However, not all forms of OPCA are types of SCA, and vice versa. This overlapping classification system is confusing and to some in the Bereich.Quelle controversy: Wikipedia

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