Search Results 31-40 of 16726 for ataxia
— Mayo Clinic researchers, along with national and global collaborators, have developed a potential test for Machado-Joseph disease, or spinocerebellar ataxia ...
The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...
... ataxia. Blood relatives include a parent, sibling or grandparent. Multiple system atrophy (MSA) is not known to be passed down through families. A family ...
Angelman syndrome · Friedreich's ataxia · Mitochondrial disorders · Neurogenetics ...
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disease with no disease modifying treatments or therapies available. Patients ...
Examples of other genetic diagnoses include: Ataxia-telangiectasia. Basal cell nevus syndrome. Bloom syndrome. Carney complex. Dyskeratosis congenita. Fanconi ...
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