-
Dentatorubral–pallidoluysian
atrophy (DRPLA) is an
autosomal dominant spinocerebellar degeneration caused by an
expansion of a CAG
repeat encoding a polyglutamine...
- 260–266. doi:10.1093/ageing/afp020. PMID 19276093. Tsuji, S. (1999). "
Dentatorubral-pallidoluysian atrophy:
Clinical features and
molecular genetics". Adv...
- the
spinocerebellar ataxias type 1, 3 and 17, neuroacanthocytosis,
dentatorubral-pallidoluysian
atrophy (DRPLA),
brain iron ac****ulation disorders, Wilson's...
-
dyssynergia cerebellaris myoclonica,
dyssynergia cerebellaris progressiva,
dentatorubral degeneration, or
Ramsay Hunt
cerebellar syndrome.
Onset of symptoms...
-
Other autosomal dominant diseases that can be
misdiagnosed as HD are
dentatorubral-pallidoluysian
atrophy and neuroferritinopathy. Also, some autosomal...
-
trinucleotide repeat disorder known as "
dentatorubral-pallidoluysian atrophy" or "dentatorubropallidoluysian atrophy".
Dentatorubral-pallidoluysian
atrophy (DRPLA)...
-
Purkinje cells send
their afferents to the
ipsilateral dentate nucleus.
Dentatorubral tract fibers: the
dentate nucleus afferents travel via the superior...
-
disease and
Huntington disease-like 2, spinal-bulbar
muscular atrophy,
dentatorubral-pallidoluysian atrophy, and
spinocerebellar ataxia 1–3, 6–8, and 17...
- C9orf72,
spinocerebellar ataxias type 1 and 3, neuroacanthocytosis,
dentatorubral-pallidoluysian
atrophy (DRPLA),
brain iron ac****ulation disorders, Wilson's...
- SCA28, SCA32, SCA34-SCA37,
autosomal dominant cerebellar ataxia and
dentatorubral pallidoluysian atrophy. Type I ADCA is
characterized by
different symptoms...
