- irreversible. It
accounts for 40% of
ataxias of
unknown origin and 15% of all
ataxias. Less than 10% of
people with
gluten ataxia present any gastrointestinal...
- Charcot-Marie-Tooth
types 1 and 2,
ataxia with
vitamin E deficiency,
ataxia-oculomotor
apraxia types 1 and 2, and
other early-onset
ataxias.
Physicians and patients...
-
system atrophy).
Gluten ataxia accounts for 40% of all
sporadic idiopathic ataxias and 15% of all
ataxias.
Primary auto-immune
ataxias (PACA) lack diagnostic...
- ****ation. The
hereditary ataxias are
categorized by mode of
inheritance and
causative gene or
chromosomal locus. The
hereditary ataxias can be
inherited in...
-
medication has been
approved for the
treatment of
inherited cerebellar ataxias,
including Ataxia-Telangiectasia. Nonetheless, a new
study that
identified retroelement...
- that they may also be
present in
other cerebellar ataxias can make
diagnosis difficult.
Other ataxias may also have
symptoms that
affect gait, speech,...
-
Spinocerebellar ataxia type 1 (SCA1) is a rare
autosomal dominant disorder, which, like
other spinocerebellar ataxias, is
characterized by neurological...
-
Locomotor ataxia is the
inability to
precisely control one's own
bodily movements.
People afflicted with this
disease may walk in a jerky, non-fluid manner...
- Mov. Disord. 19 (1): 113–4. doi:10.1002/mds.20014. PMID 14743372. S2CID 33805112.
Spinocerebellar Ataxias including Machado-Joseph
Disease at NINDS...
-
Sensory ataxia is both a
symptom and a sign in neurology. It is a form of
ataxia (loss of coordination)
caused not by
cerebellar dysfunction but by loss...
