Dentatorubral-pallidoluysian atrophy (DRPLA) presenting with psychosis

Journal of Neuropsychiatry and Clinical Neurosciences

Volumn 13, Issue 2, 2001, Pages 258-260

  Adachi, N ^a   Arima, K ^a   Asada, T ^a   Kato, M ^a   Minami, N ^a   Goto, Y I ^a   Onuma, T ^a   Ikeuchi, T ^a   Tsuji, S ^a   Hayashi, M ^a   Fukutani, Y ^a  

^a Adachi Mental Clinic   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; DELUSION; DENTATORUBROPALLIDOLUYSIAN ATROPHY; EXTRAPYRAMIDAL SYMPTOM; FEMALE; GENETIC ANALYSIS; HUMAN; JAPAN; MALE; PRIORITY JOURNAL; PSYCHOSIS;

EID: 0034989126     PISSN: 08950172     EISSN: None     Source Type: Journal    
DOI: 10.1176/jnp.13.2.258     Document Type: Article

References (10)

1. Dentatorubral-pallidoluysian atrophy: Clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat
2. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
3. Geographical distribution of origins of DRPLA family in Japan, and prevalence of DRPLA in Niigata prefecture
4. Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
5. Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathological variants in a family
6. Clinical psychopathology of dentatorubropallidoluysian atrophy
7. A family of dentatorubropallidoluysian atrophy (DRPLA) including two cases with schizophrenic symptoms
8. Four cases of progressive myoclonus epilepsy with paranoid state
9. Dentatorubral-pallidoluysian atrophy and Haw Rever syndrome
10. A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families