Sleep in patients with primary dystonia: A systematic review on the state of research and perspectives

Hertenstein, Elisabeth; Tang, Nicole K. Y.; Bernstein, Celia J.; Nissen, Christoph; Underwood, Martin; Sandhu, Harbinder

doi:10.1016/j.smrv.2015.04.004

Cited by 56 publications

(56 citation statements)

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“…Dystonia, Parkinsonian rigidity, tics, chorea, and athetosis are always abolished by sleep (40, 41). The exploration of the influence of sleep should therefore be a focus of all dystonia management plans (42–44) and may be considered the “ poor man’s examination under anesthesia .”…”

Section: An Unmet Need To Recognize That Dystonia Is Abolished By Slementioning

confidence: 99%

“…The comorbidity of non-motor symptoms is increasingly recognized in adults with dystonia (64, 65). It is not known, if these non-motor symptoms, including poor sleep patterns (41), are intrinsic to dystonia comorbidities or secondary to the dystonia disorders themselves. Understanding the role of non-motor symptoms in childhood dystonia has potential implications for clinical assessment tools; pre- and post-surgical interventions, e.g., deep brain stimulation (DBS), and treatment targets.…”

Section: The Need To Recognize Non-motor Symptoms In Childhood Dystoniamentioning

confidence: 99%

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Recognizing the Common Origins of Dystonia and the Development of Human Movement: A Manifesto of Unmet Needs in Isolated Childhood Dystonias

Lin

Nardocci

2016

Front. Neurol.

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Dystonia in childhood may be severely disabling and often unremitting and unrecognized. Considered a rare disorder, dystonic symptoms in childhood are pervasive in many conditions including disorders of developmental delay, cerebral palsy (CP), autism, neurometabolic, neuroinflammatory, and neurogenetic disorders. Collectively, there is a need to recognize the role of early postures and movements which characterize phases of normal fetal, infant, and child development as a backdrop to the many facets of dystonia in early childhood neurological disorders and to be aware of the developmental context of dystonic symptoms. The role of cocontraction is explored throughout infancy, childhood, young adulthood, and in the elderly. Under-recognition of pervasive dystonic disorders of childhood, including within CP is reviewed. Original descriptions of CP by Gowers are reviewed and contemporary physiological demonstrations are used to illustrate support for an interpretation of the tonic labyrinthine response as a manifestation of dystonia. Early recognition and molecular diagnosis of childhood dystonia where possible are desirable for appropriate clinical stratification and future precision medicine and functional neurosurgery where appropriate. A developmental neurobiological perspective could also be useful in exploring new clinical strategies for adult-onset dystonia disorders focusing on environmental and molecular interactions and systems behaviors.

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Section: An Unmet Need To Recognize That Dystonia Is Abolished By Slementioning

confidence: 99%

Section: The Need To Recognize Non-motor Symptoms In Childhood Dystoniamentioning

confidence: 99%

Recognizing the Common Origins of Dystonia and the Development of Human Movement: A Manifesto of Unmet Needs in Isolated Childhood Dystonias

Lin

Nardocci

2016

Front. Neurol.

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“…G. Heiman и R. Ottman [5] опубликовали данные, доказывающие, что депрессия чаще встречается у носителей мутации дистонии DYT1 при отсутствии клинических проявлений гиперкинеза. Имеются сообщения [6] о высокой частоте нарушений сна у больных c МД. Заболевание значительно ухудшает физические и психологические составляющие качества жизни пациентов с дистоническими гиперкинезами [7,8].…”

unclassified

Emotional and personality characteristics of patients with dystonia

Чернуха

Tarasevich

2017

Z. nevrol. psikhiatr. im. S.S. Korsakova

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Higher levels of anxiety and depression in patients with dystonia compared to the control groups were identified. The level of anxiety and depression was not correlated with disease severity. Personality profile study confirmed the high level of anxiety in patients with dystonia and additionally showed increased emotional instability and poor emotional control. Intellectual personality characteristics of patients with dystonia had no differences compared to the control groups. An analysis of socio-psychological characteristics of personality in patients with dystonia and GFS showed restricted interpersonal and social communications since the motor defect noticeable to others leads to severe social exclusion and the desire for self-isolation.

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“…Качество жизни при цервикальной дистонии [5], диссомнией [6] и тревожно-депрессивным расстройством. Боль -наиболее частый коморбидный синдром при ЦД, встречающийся у 70% пациентов [7].…”

Section: Introductionunclassified