Mood disorder affects age at onset of adult-onset cervical dystonia
نویسندگان
چکیده
منابع مشابه
Nonmotor symptoms in primary adult‐onset cervical dystonia and blepharospasm
BACKGROUND The nature and frequency of nonmotor symptoms in primary adult-onset cervical dystonia (CD) and blepharospasm (BSP) patients in Chinese populations remain unknown. METHODS Hamilton's Depression Scale (HAMD), Hamilton's Anxiety Scale (HAMA), Addenbrooke's Cognitive Examination Revised (ACE-R), Pittsburgh Sleep Quality Index and Epworth Sleepiness Scale were used to evaluate NMS in 1...
متن کاملDystonia-predominant adult-onset Huntington disease: association between motor phenotype and age of onset in adults.
BACKGROUND In juvenile Huntington disease (HD), dystonia as well as parkinsonism and eye movement abnormalities may be the predominant motor signs rather than chorea. Several patients have come to our attention with adult-onset HD in whom there is prominent dystonia and minimal chorea (ie, an adult-onset form of HD that resembles juvenile HD). OBJECTIVES To estimate the prevalence of these ca...
متن کاملA variant of adult-onset torsion dystonia?
SYNOPSIS Thirty-nine patients with the idiopathic blepharospasm-oromandibular dystonia syndrome are described. All presented in adult life, usually in the sixth decade; women were more commonly affected than men. Thirteen had blepharospasm alone, nine had oromandibular dystonia alone, and 17 had both. Torticollis or dystonic writer's cramp preceded the syndrome in two patients. Eight other pati...
متن کاملDoes sex influence age at onset in cranial-cervical and upper limb dystonia?
The relation between age at dystonia onset and sex was investigated in 264 patients with cranial-cervical dystonia and 56 patients with upper limb dystonia. In cranial-cervical dystonia, women had a significantly greater age at the onset of dystonia than men. The association was independent of duration of disease and distance of referral, but it was no longer detectable after adjustment for edu...
متن کاملAdult-onset dystonia in Aicardi-Goutières syndrome.
Aicardi-Goutières syndrome (AGS) is a rare, genetically determined encephalopathy with features mimicking congenital infection (microcephaly, bilateral basal ganglia calcifications, cerebral white matter abnormalities, cerebral atrophy, chronic CSF lymphocytosis, and elevated CSF INF-a). Disease onset usually occurs during the first year of life as a subacute encephalopathy and then the clinica...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Clinical Parkinsonism & Related Disorders
سال: 2020
ISSN: 2590-1125
DOI: 10.1016/j.prdoa.2020.100049