- Dentatorubral–pallidoluysian
atrophy (
DRPLA) is an
autosomal dominant spinocerebellar degeneration caused by an
expansion of a CAG
repeat encoding a polyglutamine...
-
tissue observed in
those afflicted with
DRPLA.
There are both juvenile-onset and late adult-onset
variants of
DRPLA,
which show
differing degrees of severity...
- 1, 3 and 17, neuroacanthocytosis, dentatorubral-pallidoluysian
atrophy (
DRPLA),
brain iron ac****ulation disorders, Wilson's disease,
benign hereditary...
-
Medicine Medical Subject Headings (MeSH) GeneReviews/NCBI/NIH/UW
entry on
DRPLA National Institute of
Neurological Disorders and
Stroke Archived 2016-12-15...
- adult-onset
DRPLA is
characterized by ataxia, c****oathetosis and dementia.
Early adult-onset
DRPLA also
includes seizures and myoclonus. Juvenile-onset
DRPLA presents...
- type 1 and 3, neuroacanthocytosis, dentatorubral-pallidoluysian
atrophy (
DRPLA),
brain iron ac****ulation disorders, Wilson's disease,
benign hereditary...
-
neurological dysfunction in a
patient with dentatorubral-pallidoluysian
atrophy (
DRPLA)".
Epilepsy Behav Case Rep. 8: 44–46. doi:10.1016/j.ebcr.2017.05.004. PMC 5565628...
- (DPT vaccine) DRE
Digital Rectal ExaminationDilated Retinal Exam
DRPLA Dentatorubral-Pallidoluysian
Atrophy DRT dead
right there DS
disease Down...
- effects.
Within the
first subclass of Type 1 are SCA1, SCA2, SCA3, SCA17, and
DRPLA. This
first subclass is the most
common of Type 1
ADCAs with SCA3 being...
- dentatorubral–pallidoluysian
atrophy (
trinucleotide expansion in the
DRPLA gene),
spinocerebellar ataxia type 1 (
trinucleotide expansion in the SCA1gene)...
