Neuropsychiatric and sleep study in autosomal dominant dopa-responsive dystonia

Although the diurnal fluctuation of motor dysfunction, reversible with small doses of dopamine, is a cornerstone for the phenotype of the autosomal dominant Segawa syndrome, the non-motor symptoms of this neurotransmitter deficiency have still received limited attention. This study aims to evaluate...

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Bibliographic Details
Published in:	Molecular genetics and metabolism reports Vol. 31; p. 100870
Main Authors:	Alves Júnior, Ailton C., Daker, Maurício V., Machado, Alexei M.C., Luna, Alan S., Valladares Neto, Dirceu C., Valadares, Eugenia R.
Format:	Journal Article
Language:	English
Published:	Elsevier Inc 01-06-2022 Elsevier
Subjects:	Autosomal dominant familial dystonia Autosomal dominant GPCH1 deficiency Dystonia, Dopa-responsive Dystonic disorders Mental disorders Research Paper Sleep-wake disorders ADHD CHD Mental disorders Autosomal dominant GPCH1 deficiency HGNC 4193 DYT5a WMT-2 MDE Dystonia, Dopa-responsive Sleep-wake disorders SG GTP Cyclohydrolase-1 BDI-II MINI/MINI PLUS WHOQOL-BREF DYT/PARK-GCH1 NSG ESS GCH1 Autosomal dominant familial dystonia GAD MDE PAST BH4 Dystonic disorders NMS L-Dopa DRD PSQI
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