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Spinocerebellar ataxia (SCA) is a progressive, degenerative,
genetic disease with
multiple types, each of
which could be
considered a
neurological condition...
- The
spinocerebellar tracts are
nerve tracts originating in the
spinal cord and
terminating in the same side (ipsilateral) of the cerebellum. The two main...
- Machado–Joseph
Azorean disease, Machado's disease, Joseph's
disease or
spinocerebellar ataxia type 3 (SCA3), is a rare
autosomal dominantly inherited neurodegenerative...
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Spinocerebellar ataxia type 1 (SCA1) is a rare
autosomal dominant disorder, which, like
other spinocerebellar ataxias, is
characterized by neurological...
- ****anese diarist. She
wrote about her
personal experiences living with
spinocerebellar ataxia which was
later published in the book 1
Litre no Namida. The...
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travels up the
spinal cord in the
ventral spinocerebellar tract. Also
known as the
anterior spinocerebellar tract,
sensory receptors take in the information...
-
Spinocerebellar ataxia type 6 (SCA6) is a rare, late-onset,
autosomal dominant disorder, which, like
other types of SCA, is
characterized by dysarthria...
- area in
front of the
posterior column and
medial to the
posterior spinocerebellar tract.
Descending motor pathways carry motor signals from the brain...
- It
consists of
fibers from the four
spinocerebellar tracts that
enter the cerebellum:
Posterior spinocerebellar tract:
unconscious proprioceptive information...
-
especially the
nervous system. Clinically,
patients may
present with
spinocerebellar ataxia, polyneuropathy,
muscle weakness, and retinopathy. Diagnosis...
