Tremor in X-linked recessive spinal and bulbar muscular atrophy (Kennedy's disease)
Clinics
;
66(6): 955-957, 2011. tab
Article
Dans Anglais
| LILACS
| ID: lil-594361
ABSTRACT
OBJECTIVE:
To study tremor in patients with X-linked recessive spinobulbar muscular atrophy or Kennedy's disease.METHODS:
Ten patients (from 7 families) with a genetic diagnosis of Kennedy's disease were screened for the presence of tremor using a standardized clinical protocol and followed up at a neurology outpatient clinic. All index patients were genotyped and showed an expanded allele in the androgen receptor gene.RESULTS:
Mean patient age was 37.6 years and mean number of CAG repeats 47 (44-53). Tremor was present in 8 (80 percent) patients and was predominantly postural hand tremor. Alcohol responsiveness was detected in 7 (88 percent) patients with tremor, who all responded well to treatment with a β-blocker (propranolol).CONCLUSION:
Tremor is a common feature in patients with Kennedy's disease and has characteristics similar to those of essential tremor.
Texte intégral:
Disponible
Indice:
LILAS (Amériques)
Sujet Principal:
Tremblement
/
Amyotrophie bulbospinale liée à l'X
Type d'étude:
Guide de pratique
Limites du sujet:
Adulte
/
Humains
/
Mâle
langue:
Anglais
Texte intégral:
Clinics
Thème du journal:
Médicament
Année:
2011
Type:
Article
Pays d'affiliation:
Brésil
Institution/Pays d'affiliation:
Genetika Laboratory/BR
/
University of Paraná/BR
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