- The
spinocerebellar tracts are
nerve tracts originating in the
spinal cord and
terminating in the same side (ipsilateral) of the cerebellum. The two main...
-
Spinocerebellar ataxia (SCA) is a progressive, degenerative,
genetic disease with
multiple types, each of
which could be
considered a
neurological condition...
-
Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset,
autosomal dominant disorder, which, like
other types of SCA, is
characterized by dysarthria...
-
Spinocerebellar ataxia type 1 (SCA1) is a rare
autosomal dominant disorder, which, like
other spinocerebellar ataxias, is
characterized by neurological...
- Machado–Joseph
Azorean disease, Machado's disease, Joseph's
disease or
spinocerebellar ataxia type 3 (SCA3), is a rare
autosomal dominantly inherited neurodegenerative...
-
travels up the
spinal cord in the
ventral spinocerebellar tract. Also
known as the
anterior spinocerebellar tract,
sensory receptors take in the information...
-
anemia and
spinocerebellar ataxia is a very rare
genetic disorder which is
characterized by mild
sideroblastic anemia, and
spinocerebellar ataxia that...
- ****anese diarist. She
wrote about her
personal experiences living with
spinocerebellar ataxia which was
later published in the book 1
Litre no Namida. The...
- spinal-bulbar
muscular atrophy, dentatorubral-pallidoluysian atrophy, and
spinocerebellar ataxia 1–3, 6–8, and 17. The
first main category, the loss of function...
- that in
humans is
encoded by the ATXN2 gene.
Mutations in ATXN2
cause spinocerebellar ataxia type 2 (SCA2). Ataxin-2
contains the
following protein domains:...
