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This form is used to provide required information for the verification of Student/Spouse living allowances as part of the 2011-2012 Free Application for Federal Student Aid (FAFSA).
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How to fill out SCA12
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Download the SCA12 form from the official website.
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Individuals who are seeking to apply for a specific service or program requiring the SCA12 form.
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Those needing to report certain information to a regulatory body or agency.
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People Also Ask about
Is SCA12 curable?
Spinocerebellar ataxia (SCA) comprises more than 40 types of similar inherited brain disorders. SCA affects your cerebellum, a part of your brain vital to physical movement. It causes problems with coordination and movement. There's no cure, so treatment aims to relieve symptoms and improve function.
What is the prognosis for SCA2?
Signs and symptoms of the disorder typically begin in mid-adulthood but can appear anytime from childhood to late adulthood. People with SCA2 usually survive 10 to 20 years after symptoms first appear.
Is SCA12 curable?
Spinocerebellar ataxia (SCA) comprises more than 40 types of similar inherited brain disorders. SCA affects your cerebellum, a part of your brain vital to physical movement. It causes problems with coordination and movement. There's no cure, so treatment aims to relieve symptoms and improve function.
How rare is SCA2?
How common is SCA2? SCA2 is about twice as common as SCA1 which appears in approximately 1 to 2 people in 100,000. (The ratio varies based on geographical location and ethnic background.) Overall, it accounts for about 13 percent of the autosomal dominant cerebellar ataxias.
What is SCA12 disease?
Spinocerebellar Ataxia type 12 (SCA12) is a rare neurodegenerative disorder. It is caused by a CAG triplet repeat expansion in the PPP2R2B gene. SCA12 is very rare worldwide. However, SCA12 is very prevalent in Northern India. Approximately 16% of autosomal dominant ataxia patients in India have SCA12.
What are the symptoms of SCA2?
People with this condition initially experience problems with coordination and balance (ataxia). Other early signs and symptoms of SCA2 include additional movement problems, speech and swallowing difficulties, and weakness in the muscles that control eye movement (ophthalmoplegia).
What is the age of SCA12 onset?
The age of symptomatic onset ranges from 8 to 55 years with most patients presenting in the 4th decade. Like SCA8 the pathogenesis of SCA12 seems to be related to a toxic effect at the RNA level as it is caused by a CAG expansion at the 5' end of the PPP2R2B gene on chromosome 5q31-5q32. Prognosis is essentially good.
How rare is SCA2?
How common is SCA2? SCA2 is about twice as common as SCA1 which appears in approximately 1 to 2 people in 100,000. (The ratio varies based on geographical location and ethnic background.) Overall, it accounts for about 13 percent of the autosomal dominant cerebellar ataxias.
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What is SCA12?
SCA12 is a form used to report and declare certain types of income or transactions for tax purposes to ensure compliance with tax regulations.
Who is required to file SCA12?
Individuals and entities that engage in specific types of transactions or receive certain forms of income that must be reported to tax authorities are required to file SCA12.
How to fill out SCA12?
To fill out SCA12, obtain the form from the relevant tax authority, provide accurate information regarding your income or transactions, and follow the instructions to ensure all sections are completed correctly.
What is the purpose of SCA12?
The purpose of SCA12 is to facilitate the reporting of specific income, ensuring transparency and compliance with tax laws, and aiding in the accurate assessment of tax obligations.
What information must be reported on SCA12?
The information that must be reported on SCA12 typically includes personal identification details, descriptions of the income or transactions, amounts involved, dates, and any other relevant financial information.
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