Ad
related to: sca aphasia classification scale table printable sheet 1 12workbook-aphasia.pdffiller.com has been visited by 1M+ users in the past month
- Type Text in PDF Online
Upload & Type on PDF Files Online.
No Installation Needed. Try Now!
- pdfFiller Account Log In
Easily Sign Up or Login to Your
pdfFiller Account. Try Now!
- Write Text in PDF Online
Upload & Write on PDF Forms Online.
No Installation Needed. Try Now!
- Convert PDF to Word
Convert PDF to Editable Online.
No Installation Needed. Try Now!
- Type Text in PDF Online
Search results
Results from the WOW.Com Content Network
Spinocerebellar ataxia (SCA) is a progressive, degenerative, [1] genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time. SCA is hereditary, progressive, degenerative, and often ...
Spinocerebellar ataxia type 1 (SCA1) is a rare autosomal dominant disorder, which, like other spinocerebellar ataxias, is characterized by neurological symptoms including dysarthria, hypermetric saccades, and ataxia of gait and stance.
The Boston Diagnostic Aphasia Examination provides a comprehensive exploration of a range of communicative abilities. Its results are used to classify patient's language profiles into one of the localization based classifications of aphasia: Broca's, Wernicke's, anomic, conduction, transcortical, transcortical motor, transcortical sensory, and global aphasia syndromes, although the test does ...
The updated version is the Western Aphasia Battery-Revised (WAB-R). [1] The battery helps discern the presence, degree, and type of aphasia. It can provide a baseline for monitoring changes during therapy. It is useful for determining what to treat. It can provide indications of the location of the lesion that caused the aphasia. [2]
Spinocerebellar ataxia type 13 (SCA13) is a rare autosomal dominant disorder, which, like other types of SCA, is characterized by dysarthria, nystagmus, and ataxia of gait, stance and the limbs due to cerebellar dysfunction.
The Boston Naming Test (BNT), introduced in 1983 by Edith Kaplan, Harold Goodglass and Sandra Weintraub, is a widely used neuropsychological assessment tool to measure confrontational word retrieval in individuals with aphasia or other language disturbance caused by stroke, Alzheimer's disease, or other dementing disorder. [1]
FRDA is the most prevalent inherited ataxia, affecting approximately 1 in 40,000 with European descent. [15] Males and females are affected equally. The estimated carrier prevalence is 1:100. [5] A 1990–1996 study of Europeans calculated the incidence rate was 2.8:100,000. [40] The prevalence rate of FRDA in Japan is 1:1,000,000. [41]
In Germany, SCA6 accounts for 10-25% of all autosomal dominant cases of SCA (SCA itself having a prevalence of 1 in 100,000). [8] [9] This prevalence in lower in Japan, however, where SCA6 accounts for only ~6% of spinocerebellar ataxias. [10] In Australia, SCA6 accounts for 30% of spinocerebellar ataxia cases while 11% in the Dutch. [11] [12]
Ad
related to: sca aphasia classification scale table printable sheet 1 12workbook-aphasia.pdffiller.com has been visited by 1M+ users in the past month