Sleep disorders in Wilson’s disease: a questionnaire study

Objective To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and investigate its potential mechanisms. Methods A total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matc...

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Published inNeurological sciences Vol. 44; no. 1; pp. 209 - 214
Main Authors You, Zhifei, Xu, Hui, Wu, Zhonghua, You, Zhengchen
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.01.2023
Springer Nature B.V
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ISSN1590-1874
1590-3478
1590-3478
DOI10.1007/s10072-022-06401-4

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Abstract Objective To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and investigate its potential mechanisms. Methods A total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matched control subjects were investigated using 3 standardized sleep questionnaires. Differences among 3 subtypes were discussed. Results The mean Parkinson’s disease sleep scale (PDSS) score of WD was lower than the controls ( Z  =  − 4.426, P  = 0.000), and their mean Epworth Sleepiness Scale (ESS) score as well as Pittsburgh sleep quality index (PSQI) score of WD was higher than that of the controls ( t  = 2.005, P  = 0.048; t  = 3.342, P  = 0.001). The incidence of excessive daytime sleepiness (EDS) in WD group were significantly higher than the controls ( X 2  = 6.064, P  = 0.014). Further analysis showed that total PDSS score of neurologic presentation group was lower than others ( X 2  = 6.131, P  = 0.047), while the ESS score was higher ( F  = 3.817, P  = 0.029). UWDRS showed a negative correlation with PDSS ( r  =  − 0.440, P  = 0.022) and has a higher negative correlation with PDSS in neurologic presentation group ( r  =  − 0.732, P  = 0.000). Conclusions Patients with WD often suffer from sleep disturbances, mainly characterized by difficulty falling asleep, difficulty staying asleep, nocturnal motor symptoms (numbness, cramps, tremor), and daytime dozing. And the incidence of EDS is significantly higher than that of the controls. Sleep quality is worse in patients with WD of neurologic presentation than the other two groups. Furthermore, the worse of the symptoms, patients with WD suffer more serious of the sleep disorders especially in neurologic presentation group.
AbstractList To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson's disease (WD), and investigate its potential mechanisms.OBJECTIVETo examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson's disease (WD), and investigate its potential mechanisms.A total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matched control subjects were investigated using 3 standardized sleep questionnaires. Differences among 3 subtypes were discussed.METHODSA total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matched control subjects were investigated using 3 standardized sleep questionnaires. Differences among 3 subtypes were discussed.The mean Parkinson's disease sleep scale (PDSS) score of WD was lower than the controls (Z =  - 4.426, P = 0.000), and their mean Epworth Sleepiness Scale (ESS) score as well as Pittsburgh sleep quality index (PSQI) score of WD was higher than that of the controls (t = 2.005, P = 0.048; t = 3.342, P = 0.001). The incidence of excessive daytime sleepiness (EDS) in WD group were significantly higher than the controls (X2 = 6.064, P = 0.014). Further analysis showed that total PDSS score of neurologic presentation group was lower than others (X2 = 6.131, P = 0.047), while the ESS score was higher (F = 3.817, P = 0.029). UWDRS showed a negative correlation with PDSS (r =  - 0.440, P = 0.022) and has a higher negative correlation with PDSS in neurologic presentation group (r =  - 0.732, P = 0.000).RESULTSThe mean Parkinson's disease sleep scale (PDSS) score of WD was lower than the controls (Z =  - 4.426, P = 0.000), and their mean Epworth Sleepiness Scale (ESS) score as well as Pittsburgh sleep quality index (PSQI) score of WD was higher than that of the controls (t = 2.005, P = 0.048; t = 3.342, P = 0.001). The incidence of excessive daytime sleepiness (EDS) in WD group were significantly higher than the controls (X2 = 6.064, P = 0.014). Further analysis showed that total PDSS score of neurologic presentation group was lower than others (X2 = 6.131, P = 0.047), while the ESS score was higher (F = 3.817, P = 0.029). UWDRS showed a negative correlation with PDSS (r =  - 0.440, P = 0.022) and has a higher negative correlation with PDSS in neurologic presentation group (r =  - 0.732, P = 0.000).Patients with WD often suffer from sleep disturbances, mainly characterized by difficulty falling asleep, difficulty staying asleep, nocturnal motor symptoms (numbness, cramps, tremor), and daytime dozing. And the incidence of EDS is significantly higher than that of the controls. Sleep quality is worse in patients with WD of neurologic presentation than the other two groups. Furthermore, the worse of the symptoms, patients with WD suffer more serious of the sleep disorders especially in neurologic presentation group.CONCLUSIONSPatients with WD often suffer from sleep disturbances, mainly characterized by difficulty falling asleep, difficulty staying asleep, nocturnal motor symptoms (numbness, cramps, tremor), and daytime dozing. And the incidence of EDS is significantly higher than that of the controls. Sleep quality is worse in patients with WD of neurologic presentation than the other two groups. Furthermore, the worse of the symptoms, patients with WD suffer more serious of the sleep disorders especially in neurologic presentation group.
ObjectiveTo examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and investigate its potential mechanisms.MethodsA total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matched control subjects were investigated using 3 standardized sleep questionnaires. Differences among 3 subtypes were discussed.ResultsThe mean Parkinson’s disease sleep scale (PDSS) score of WD was lower than the controls (Z =  − 4.426, P = 0.000), and their mean Epworth Sleepiness Scale (ESS) score as well as Pittsburgh sleep quality index (PSQI) score of WD was higher than that of the controls (t = 2.005, P = 0.048; t = 3.342, P = 0.001). The incidence of excessive daytime sleepiness (EDS) in WD group were significantly higher than the controls (X2 = 6.064, P = 0.014). Further analysis showed that total PDSS score of neurologic presentation group was lower than others (X2 = 6.131, P = 0.047), while the ESS score was higher (F = 3.817, P = 0.029). UWDRS showed a negative correlation with PDSS (r =  − 0.440, P = 0.022) and has a higher negative correlation with PDSS in neurologic presentation group (r =  − 0.732, P = 0.000).ConclusionsPatients with WD often suffer from sleep disturbances, mainly characterized by difficulty falling asleep, difficulty staying asleep, nocturnal motor symptoms (numbness, cramps, tremor), and daytime dozing. And the incidence of EDS is significantly higher than that of the controls. Sleep quality is worse in patients with WD of neurologic presentation than the other two groups. Furthermore, the worse of the symptoms, patients with WD suffer more serious of the sleep disorders especially in neurologic presentation group.
Objective To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and investigate its potential mechanisms. Methods A total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matched control subjects were investigated using 3 standardized sleep questionnaires. Differences among 3 subtypes were discussed. Results The mean Parkinson’s disease sleep scale (PDSS) score of WD was lower than the controls ( Z  =  − 4.426, P  = 0.000), and their mean Epworth Sleepiness Scale (ESS) score as well as Pittsburgh sleep quality index (PSQI) score of WD was higher than that of the controls ( t  = 2.005, P  = 0.048; t  = 3.342, P  = 0.001). The incidence of excessive daytime sleepiness (EDS) in WD group were significantly higher than the controls ( X 2  = 6.064, P  = 0.014). Further analysis showed that total PDSS score of neurologic presentation group was lower than others ( X 2  = 6.131, P  = 0.047), while the ESS score was higher ( F  = 3.817, P  = 0.029). UWDRS showed a negative correlation with PDSS ( r  =  − 0.440, P  = 0.022) and has a higher negative correlation with PDSS in neurologic presentation group ( r  =  − 0.732, P  = 0.000). Conclusions Patients with WD often suffer from sleep disturbances, mainly characterized by difficulty falling asleep, difficulty staying asleep, nocturnal motor symptoms (numbness, cramps, tremor), and daytime dozing. And the incidence of EDS is significantly higher than that of the controls. Sleep quality is worse in patients with WD of neurologic presentation than the other two groups. Furthermore, the worse of the symptoms, patients with WD suffer more serious of the sleep disorders especially in neurologic presentation group.
To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson's disease (WD), and investigate its potential mechanisms. A total of 150 patients with WD (76 hepatic, 42 neurological, 32 asymptomatic form) and 150 age- and sex-matched control subjects were investigated using 3 standardized sleep questionnaires. Differences among 3 subtypes were discussed. The mean Parkinson's disease sleep scale (PDSS) score of WD was lower than the controls (Z =  - 4.426, P = 0.000), and their mean Epworth Sleepiness Scale (ESS) score as well as Pittsburgh sleep quality index (PSQI) score of WD was higher than that of the controls (t = 2.005, P = 0.048; t = 3.342, P = 0.001). The incidence of excessive daytime sleepiness (EDS) in WD group were significantly higher than the controls (X  = 6.064, P = 0.014). Further analysis showed that total PDSS score of neurologic presentation group was lower than others (X  = 6.131, P = 0.047), while the ESS score was higher (F = 3.817, P = 0.029). UWDRS showed a negative correlation with PDSS (r =  - 0.440, P = 0.022) and has a higher negative correlation with PDSS in neurologic presentation group (r =  - 0.732, P = 0.000). Patients with WD often suffer from sleep disturbances, mainly characterized by difficulty falling asleep, difficulty staying asleep, nocturnal motor symptoms (numbness, cramps, tremor), and daytime dozing. And the incidence of EDS is significantly higher than that of the controls. Sleep quality is worse in patients with WD of neurologic presentation than the other two groups. Furthermore, the worse of the symptoms, patients with WD suffer more serious of the sleep disorders especially in neurologic presentation group.
Author Wu, Zhonghua
You, Zhifei
Xu, Hui
You, Zhengchen
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  fullname: You, Zhifei
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  surname: Xu
  fullname: Xu, Hui
  organization: Department of Neurosurgery, The Sixth People’s Hospital of Nantong
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  givenname: Zhonghua
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  fullname: You, Zhengchen
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  organization: Department of Emergency, Taizhou People’s Hospital
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CitedBy_id crossref_primary_10_1186_s12888_024_05493_w
crossref_primary_10_1097_WCO_0000000000001286
crossref_primary_10_1007_s11910_023_01274_2
crossref_primary_10_1097_LVT_0000000000000369
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Keywords Questionnaire study
Sleep disorders
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Wilson’s disease
Sleepiness
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References ChaudhuriKRPalSDiMarcoAWhately-SmithCBridgmanKMathewRPezzelaFRForbesAHoglBTrenkwalderCThe Parkinson’s disease sleep scale: a new instrument for assessing sleep and nocturnal disability in Parkinson’s diseaseJ Neurol Neurosurg Psychiatry20027366296351:STN:280:DC%2BD38jhs1Gkuw%3D%3D10.1136/jnnp.73.6.629
TomicADobricicVNovakovicISvetelMPekmezovicTKresojevicNPotrebicAKosticVSMutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson’s disease in SerbiaVojnosanitetski pregled Military-Med Pharm Rev201370545746210.2298/VSP1305457T
LimaMMAndersenMLReksidlerABSilvaAZagerAZanataSMVitalMATufikSBlockage of dopaminergic D(2) receptors produces decrease of REM but not of slow wave sleep in rats after REM sleep deprivationBehav Brain Res200818824064111:CAS:528:DC%2BD1cXhslOju7g%3D10.1016/j.bbr.2007.11.025
FigorilliMLanzaGCongiuPLeccaRCasagliaEMogaveroMPPulighedduMFerriRNeurophysiological aspects of REM sleep behavior disorder (RBD): a narrative reviewBrain Sci2021111215881:CAS:528:DC%2BB38XltFGqsL4%3D10.3390/brainsci11121588
LeinweberBMollerJCScheragAReunerUGuntherPLangCJSchmidtHHSchraderCBandmannOCzlonkowskaAEvaluation of the Unified Wilson’s Disease Rating Scale (UWDRS) in German patients with treated Wilson’s diseaseMov Disord2008231546210.1002/mds.21761
DongYNiWChenWJWanBZhaoGXShiZQZhangYWangNYuLXuJFSpectrum and classification of ATP7B variants in a large cohort of Chinese patients with Wilson’s disease guides genetic diagnosisTheranostics2016656386491:CAS:528:DC%2BC28XhtlensLzK10.7150/thno.14596
FrancaASLobao-SoaresBMuratoriLNascimentoGWinneJPereiraCMJeronimoSMRibeiroSD2 dopamine receptor regulation of learning, sleep and plasticityEur Neuropsychopharmacol20152544935041:CAS:528:DC%2BC2MXhvVOru74%3D10.1016/j.euroneuro.2015.01.011
GromadzkaGTarnackaBFlagaAAdamczykACopper dyshomeostasis in neurodegenerative diseases—therapeutic implicationsInt J Mol Sci2020212392591:CAS:528:DC%2BB3MXotFeksw%3D%3D10.3390/ijms21239259
WestermarkKTedroffJThuomasKÅHartvigPLångströmBAnderssonYHörnfeldtKAquiloniusSMNeurological Wilson’s disease studied with magnetic resonance imaging and with positron emission tomography using dopaminergic markersMov Disord19951055966031:STN:280:DyaK28%2FmsVegsA%3D%3D10.1002/mds.870100511
PortalaKWestermarkKEkseliusLBromanJESleep in patients with treated Wilson’s disease. A questionnaire studyNordic J Psychiatry200256429129710.1080/08039480260242796
FerenciPCacaKLoudianosGMieli-VerganiGTannerSSternliebISchilskyMCoxDBerrFDiagnosis and phenotypic classification of Wilson diseaseLiver Int200323313914210.1034/j.1600-0676.2003.00824.x
DunmyreJRMashourGABoothVCoupled flip-flop model for REM sleep regulation in the ratPLoS ONE20149410.1371/journal.pone.0094481
Hermann W (2019) Classification and differential diagnosis of Wilson’s disease. Ann Trans Med 7(Suppl 2):S63
BertolaziANFagondesSCHoffLSDartoraEGMiozzoICde BarbaMEBarretoSSValidation of the Brazilian Portuguese version of the Pittsburgh Sleep Quality IndexSleep Med2011121707510.1016/j.sleep.2010.04.020
WiersCEShumayECabreraEShokri-KojoriEGladwinTESkardaECunninghamSIKimSWWongTCTomasiDReduced sleep duration mediates decreases in striatal D2/D3 receptor availability in cocaine abusersTransl Psychiatry201661:CAS:528:DC%2BC28XjvVyntbg%3D10.1038/tp.2016.14
BertolaziANFagondesSCHoffLSPedroVDMenna BarretoSSJohnsMWPortuguese-language version of the Epworth sleepiness scale: validation for use in BrazilJ Bras Pneumol200935987788310.1590/S1806-37132009000900009
LegerDStepnowskyCThe economic and societal burden of excessive daytime sleepiness in patients with obstructive sleep apneaSleep Med Rev20205110.1016/j.smrv.2020.101275
PulaiSBiswasARoyAGuinDSPanditAGangopadhyayGGhoraiPKSarkhelSSenapatiAKClinical features, MRI brain, and MRS abnormalities of drug-naive neurologic Wilson’s diseaseNeurol India201462215315810.4103/0028-3886.132349
Selvaraj VK, Keshavamurthy B (2016) Sleep dysfunction in Parkinson’s disease. J Clin Diagn Res: JCDR 10(2):Oc09–12
European Association For The Study Of The Liver (2012) EASL clinical practice guidelines: Wilson’s disease. J Hepatol 56(3):671–685
NevsimalovaSBuskovaJBruhaRKemlinkDSonkaKVitekLMarecekZSleep disorders in Wilson’s diseaseEur J Neurol20111811841901:STN:280:DC%2BC3M%2Fisl2qtA%3D%3D10.1111/j.1468-1331.2010.03106.x
NettoABSinhaSTalyABPandaSRaoSSleep in Wilson’s disease: questionnaire based studyAnn Indian Acad Neurol2011141313410.4103/0972-2327.78047
Kasztelan-SzczerbinskaBCichoz-LachHWilson’s disease: an update on the diagnostic workup and managementJ Clin Med2021102150971:CAS:528:DC%2BB3MXisFWmsbrN10.3390/jcm10215097
HuntJCoulsonEJRajnarayananROsterHVidenovicARawashdehOSleep and circadian rhythms in Parkinson’s disease and preclinical modelsMol Neurodegener202217112110.1186/s13024-021-00504-w
Zhou XX, Li XH, Chen DB, Wu C, Feng L, Chu JP, Yang ZY, Li XB, Qin H, Li GD (2018) The asymmetry of neural symptoms in Wilson’s disease patients detecting by diffusion tensor imaging, resting‐state functional MRI, and susceptibility‐weighted imaging. Brain Behav 8(5):e00930
Piano C, Mazzucchi E, Bentivoglio AR, Losurdo A, Calandra Buonaura G, Imperatori C, ... Della Marca G (2017) Wake and sleep EEG in patients with Huntington disease: an eLORETA study and review of the literature. Clin EEG Neurosc 48(1):60–71
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References_xml – reference: NettoABSinhaSTalyABPandaSRaoSSleep in Wilson’s disease: questionnaire based studyAnn Indian Acad Neurol2011141313410.4103/0972-2327.78047
– reference: TomicADobricicVNovakovicISvetelMPekmezovicTKresojevicNPotrebicAKosticVSMutational analysis of ATP7B gene and the genotype-phenotype correlation in patients with Wilson’s disease in SerbiaVojnosanitetski pregled Military-Med Pharm Rev201370545746210.2298/VSP1305457T
– reference: GromadzkaGTarnackaBFlagaAAdamczykACopper dyshomeostasis in neurodegenerative diseases—therapeutic implicationsInt J Mol Sci2020212392591:CAS:528:DC%2BB3MXotFeksw%3D%3D10.3390/ijms21239259
– reference: WiersCEShumayECabreraEShokri-KojoriEGladwinTESkardaECunninghamSIKimSWWongTCTomasiDReduced sleep duration mediates decreases in striatal D2/D3 receptor availability in cocaine abusersTransl Psychiatry201661:CAS:528:DC%2BC28XjvVyntbg%3D10.1038/tp.2016.14
– reference: Zhou XX, Li XH, Chen DB, Wu C, Feng L, Chu JP, Yang ZY, Li XB, Qin H, Li GD (2018) The asymmetry of neural symptoms in Wilson’s disease patients detecting by diffusion tensor imaging, resting‐state functional MRI, and susceptibility‐weighted imaging. Brain Behav 8(5):e00930
– reference: ChaudhuriKRPalSDiMarcoAWhately-SmithCBridgmanKMathewRPezzelaFRForbesAHoglBTrenkwalderCThe Parkinson’s disease sleep scale: a new instrument for assessing sleep and nocturnal disability in Parkinson’s diseaseJ Neurol Neurosurg Psychiatry20027366296351:STN:280:DC%2BD38jhs1Gkuw%3D%3D10.1136/jnnp.73.6.629
– reference: DongYNiWChenWJWanBZhaoGXShiZQZhangYWangNYuLXuJFSpectrum and classification of ATP7B variants in a large cohort of Chinese patients with Wilson’s disease guides genetic diagnosisTheranostics2016656386491:CAS:528:DC%2BC28XhtlensLzK10.7150/thno.14596
– reference: Selvaraj VK, Keshavamurthy B (2016) Sleep dysfunction in Parkinson’s disease. J Clin Diagn Res: JCDR 10(2):Oc09–12
– reference: BertolaziANFagondesSCHoffLSPedroVDMenna BarretoSSJohnsMWPortuguese-language version of the Epworth sleepiness scale: validation for use in BrazilJ Bras Pneumol200935987788310.1590/S1806-37132009000900009
– reference: DunmyreJRMashourGABoothVCoupled flip-flop model for REM sleep regulation in the ratPLoS ONE20149410.1371/journal.pone.0094481
– reference: PulaiSBiswasARoyAGuinDSPanditAGangopadhyayGGhoraiPKSarkhelSSenapatiAKClinical features, MRI brain, and MRS abnormalities of drug-naive neurologic Wilson’s diseaseNeurol India201462215315810.4103/0028-3886.132349
– reference: BertolaziANFagondesSCHoffLSDartoraEGMiozzoICde BarbaMEBarretoSSValidation of the Brazilian Portuguese version of the Pittsburgh Sleep Quality IndexSleep Med2011121707510.1016/j.sleep.2010.04.020
– reference: NevsimalovaSBuskovaJBruhaRKemlinkDSonkaKVitekLMarecekZSleep disorders in Wilson’s diseaseEur J Neurol20111811841901:STN:280:DC%2BC3M%2Fisl2qtA%3D%3D10.1111/j.1468-1331.2010.03106.x
– reference: HuntJCoulsonEJRajnarayananROsterHVidenovicARawashdehOSleep and circadian rhythms in Parkinson’s disease and preclinical modelsMol Neurodegener202217112110.1186/s13024-021-00504-w
– reference: FigorilliMLanzaGCongiuPLeccaRCasagliaEMogaveroMPPulighedduMFerriRNeurophysiological aspects of REM sleep behavior disorder (RBD): a narrative reviewBrain Sci2021111215881:CAS:528:DC%2BB38XltFGqsL4%3D10.3390/brainsci11121588
– reference: PortalaKWestermarkKEkseliusLBromanJESleep in patients with treated Wilson’s disease. A questionnaire studyNordic J Psychiatry200256429129710.1080/08039480260242796
– reference: European Association For The Study Of The Liver (2012) EASL clinical practice guidelines: Wilson’s disease. J Hepatol 56(3):671–685
– reference: FrancaASLobao-SoaresBMuratoriLNascimentoGWinneJPereiraCMJeronimoSMRibeiroSD2 dopamine receptor regulation of learning, sleep and plasticityEur Neuropsychopharmacol20152544935041:CAS:528:DC%2BC2MXhvVOru74%3D10.1016/j.euroneuro.2015.01.011
– reference: LegerDStepnowskyCThe economic and societal burden of excessive daytime sleepiness in patients with obstructive sleep apneaSleep Med Rev20205110.1016/j.smrv.2020.101275
– reference: WestermarkKTedroffJThuomasKÅHartvigPLångströmBAnderssonYHörnfeldtKAquiloniusSMNeurological Wilson’s disease studied with magnetic resonance imaging and with positron emission tomography using dopaminergic markersMov Disord19951055966031:STN:280:DyaK28%2FmsVegsA%3D%3D10.1002/mds.870100511
– reference: LimaMMAndersenMLReksidlerABSilvaAZagerAZanataSMVitalMATufikSBlockage of dopaminergic D(2) receptors produces decrease of REM but not of slow wave sleep in rats after REM sleep deprivationBehav Brain Res200818824064111:CAS:528:DC%2BD1cXhslOju7g%3D10.1016/j.bbr.2007.11.025
– reference: Kasztelan-SzczerbinskaBCichoz-LachHWilson’s disease: an update on the diagnostic workup and managementJ Clin Med2021102150971:CAS:528:DC%2BB3MXisFWmsbrN10.3390/jcm10215097
– reference: FerenciPCacaKLoudianosGMieli-VerganiGTannerSSternliebISchilskyMCoxDBerrFDiagnosis and phenotypic classification of Wilson diseaseLiver Int200323313914210.1034/j.1600-0676.2003.00824.x
– reference: Hermann W (2019) Classification and differential diagnosis of Wilson’s disease. Ann Trans Med 7(Suppl 2):S63
– reference: LeinweberBMollerJCScheragAReunerUGuntherPLangCJSchmidtHHSchraderCBandmannOCzlonkowskaAEvaluation of the Unified Wilson’s Disease Rating Scale (UWDRS) in German patients with treated Wilson’s diseaseMov Disord2008231546210.1002/mds.21761
– reference: Piano C, Mazzucchi E, Bentivoglio AR, Losurdo A, Calandra Buonaura G, Imperatori C, ... Della Marca G (2017) Wake and sleep EEG in patients with Huntington disease: an eLORETA study and review of the literature. Clin EEG Neurosc 48(1):60–71
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Snippet Objective To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and investigate...
To examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson's disease (WD), and investigate its...
ObjectiveTo examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and investigate its...
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SubjectTerms Daytime
Disorders of Excessive Somnolence - complications
Hepatolenticular Degeneration - complications
Hepatolenticular Degeneration - epidemiology
Humans
Medicine
Medicine & Public Health
Movement disorders
Neurodegenerative diseases
Neurology
Neuroradiology
Neurosciences
Neurosurgery
Original Article
Parkinson Disease - complications
Parkinson's disease
Psychiatry
Sleep
Sleep and wakefulness
Sleep disorders
Sleep Wake Disorders - diagnosis
Sleep Wake Disorders - epidemiology
Sleep Wake Disorders - etiology
Surveys and Questionnaires
Tremor
Wilson's disease
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Title Sleep disorders in Wilson’s disease: a questionnaire study
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