Movement Disorders Dedication
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Detrusor Sphincter Dyssynergia: a Review of Physiology, Diagnosis, and Treatment Strategies
Review Article Detrusor sphincter dyssynergia: a review of physiology, diagnosis, and treatment strategies John T. Stoffel Department of Urology, University of Michigan, Ann Arbor, MI, USA Correspondence to: John T. Stoffel, MD. Department of Urology, University of Michigan, Ann Arbor, MI, USA. Email: [email protected]. Abstract: Detrusor sphincter dyssynergia (DSD) is the urodynamic description of bladder outlet obstruction from detrusor muscle contraction with concomitant involuntary urethral sphincter activation. DSD is associated with neurologic conditions such as spinal cord injury, multiple sclerosis, and spina bifida and some of these neurogenic bladder patients with DSD may be at risk for autonomic dysreflexia, recurrent urinary tract infections, or upper tract compromise if the condition is not followed and treated appropriately. It is diagnosed most commonly during the voiding phase of urodynamic studies using EMG recordings and voiding cystourethrograms, although urethral pressure monitoring could also potentially be used. DSD can be sub-classified as either continuous or intermittent, although adoption of this terminology is not widespread. There are few validated oral pharmacologic treatment options for this condition but transurethral botulinum toxin injection have shown temporary efficacy in reducing bladder outlet obstruction. Urinary sphincterotomy has also demonstrated reproducible long term benefits in several studies, but the morbidity associated with this procedure can be high. Keywords: Detrusor sphincter dyssynergia (DSD); neurogenic bladder; urodynamics; external urinary sphincter (EUS) Submitted Nov 30, 2015. Accepted for publication Jan 05, 2016. doi: 10.3978/j.issn.2223-4683.2016.01.08 View this article at: http://dx.doi.org/10.3978/j.issn.2223-4683.2016.01.08 Introduction Physiology The human bladder has two functions—to store and During storage of urine, afferent nerves carry information empty urine. -
Acute Cerebellar Ataxia Associated with Intermittent ECG Pattern Similar to Wellens Syndrome and Transient Prominent QRS Anterior Forces
Acute cerebellar ataxia associated with intermittent ECG pattern similar to Wellens syndrome and transient prominent QRS anterior forces Andrés Ricardo Pérez-Riera, MD, PhD. Post-Graduates Advisor at Design of Studies and Scientific Writing Laboratory in the ABC Faculty of Medicine - ABC Foundation - Santo André – São Paulo – Brazil Raimundo Barbosa-Barros, MD. Specialist in Cardiology by the Brazilian Society of Cardiology (SBC) Specialist in Intensive Care by the Sociedade Brasileira de Terapia Intensiva Chief of the Coronary Center of the Hospital de Messejana Dr. Carlos Alberto Studart Gomes. Fortaleza - Brazil Adrian Baranchuk, MD FACC FRCPC Associate Professor of Medicine and Physiology - Cardiac Electrophysiology and Pacing - Director, EP Training Program - Kingston General Hospital - FAPC 3, 76 Stuart Street K7L 2V7, Kingston ON Queen's University - Canada Male patient, 56 years old, white, uncontrolled hypertension, was admitted to our emergency department (ED) with reports of sudden dizziness, headache of abrupt onset, nausea, vomiting and weakness in the lower limbs. Physical examination drew attention to the presence of manifestations suggestive of cerebellar syndrome: impaired coordination in the trunk or arms and legs, inability to coordinate balance, gait, extremity, uncontrolled or repetitive eye movements, (nystagmus), dyssynergia, dysmetria, dysdiadochokinesia, dysarthria (cerebellar ataxia). Normal myocardial necrosis markers and normal electrolytes ECO 1: anteroseptal-apical akinesis; LVEF = 30% ECO 2 (third day): -
Joint Contractures and Acquired Deforming Hypertonia in Older People
Annals of Physical and Rehabilitation Medicine 62 (2019) 435–441 Available online at ScienceDirect www.sciencedirect.com Review Joint contractures and acquired deforming hypertonia in older people: Which determinants? a,b, c d,e a Patrick Dehail *, Nathaly Gaudreault , Haodong Zhou , Ve´ronique Cressot , a,f g h Anne Martineau , Julie Kirouac-Laplante , Guy Trudel a Service de me´decine physique et re´adaptation, poˆle de neurosciences cliniques, CHU de Bordeaux, 33000 Bordeaux, France b Universite´ de Bordeaux, EA 4136, 33000 Bordeaux, France c E´cole de re´adaptation, faculte´ de me´decine et des sciences de la sante´, universite´ de Sherbrooke, Sherbrooke, Canada d Department of Biology, Faculty of Science, University of Ottawa, Ottawa, ON, Canada e Bone and Joint Research Laboratory, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada f De´partement de me´decine, division de physiatrie, universite´ Laval, Que´bec, QC, Canada g De´partement de me´decine, division de ge´riatrie, universite´ Laval, Que´bec, QC, Canada h Department of Medicine, Division of Physical Medicine and Rehabilitation, University of Ottawa, Bone and Joint Research Laboratory, The Ottawa Hospital Research Institute, Ottawa, ON, Canada A R T I C L E I N F O A B S T R A C T Article history: Joint contractures and acquired deforming hypertonia are frequent in dependent older people. The Received 29 March 2018 consequences of these conditions can be significant for activities of daily living as well as comfort and Accepted 29 October 2018 quality of life. They can also negatively affect the burden of care and care costs. -
Deformities of the Hands and Feet in Parkinsonism and Their Reversibility by Operation
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.26.1.33 on 1 February 1963. Downloaded from J. Neurol. Neurosurg. Psychiat., 1963, 26, 33 Deformities of the hands and feet in Parkinsonism and their reversibility by operation PETER GORTVAI From the National Hospital for Nervous Diseases, Queen Square, London Charcot (1877) described some aspects of the typical method using a small instrument which screws deformities of the hands and feet seen in Parkinson's directly into the skull and depends on localization disease. He likened the deformity of the hands to that of the target in the brain on the measurement of sometimes observed in chronic progressive rheu- angles in two planes. The lesions in the ventrolateral matism. He said that the differential diagnosis is nucleus of the thalamus were made by the injection usually made with ease, because in cases of Parkin- of 0 5 to 1 ml. of a mixture of Etopalin (Ciba) and sonism 'there is found neither the articular tume- kaolin. faction and stiffness, nor the osseous deposits and cracking sounds observed in nodose rheumatism'. DESCRIPTION OF THE DEFORMITIES guest. Protected by copyright. He describes the deformity of the toes as a 'griffe' (or claw), on account of the extension of the first and THE HANDS In its early and commonest stage the concomitant flexion of the second phalanges. deformity amounts to no more than a characteristic Hughlings Jackson (1899) also mentions deformity posture of the affected hand (Fig. 1). The fingers are of hands seen in some cases of Parkinsonism. He held extended at the interphalangeal joints and remarked that 'in paralysis agitans the interossei are flexed some 40° to 700 at the metacarpo-phalangeal the muscles of the hand which are preponderatingly joints. -
Neurogenic Bowel Dysfunction in Patients with Multiple Sclerosis Open Access to Scientific and Medical Research DOI
Journal name: Degenerative Neurological and Neuromuscular Disease Article Designation: Review Year: 2018 Volume: 8 Degenerative Neurological and Neuromuscular Disease Dovepress Running head verso: Preziosi et al Running head recto: Neurogenic bowel dysfunction in patients with multiple sclerosis open access to scientific and medical research DOI: http://dx.doi.org/10.2147/DNND.S138835 Open Access Full Text Article REVIEW Neurogenic bowel dysfunction in patients with multiple sclerosis: prevalence, impact, and management strategies Giuseppe Preziosi Abstract: Bowel dysfunction in patients with multiple sclerosis (MS) is highly prevalent. Ayeshah Gordon-Dixon Constipation and fecal incontinence can coexist and alternate, impacting on the patient’s quality Anton Emmanuel of life and social interactions, as well as burdening the caregivers. The cost for the health care providers is also significant, with increased number of hospital admissions, treatment-related Gastro-Intestinal Physiology Unit, University College London Hospital, costs, and hospital appointments. The origin is multifactorial, and includes alteration of neu- London, UK rological pathways, polypharmacy, behavioral elements, and ability to access the toilet. Every patient with MS should be sensitively questioned about bowel function, and red flag symptoms should prompt adequate investigations. Manipulation of life style factors and establishment of a bowel regime should be attempted in the first place, and if this fails, other measures such For personal use only. as biofeedback and transanal irrigation should be included. A stoma can improve quality of life, and is not necessarily a last-ditch option. Antegrade colonic enemas can also be an effec- tive option, whilst neuromodulation has not proved its role yet. Effective treatment of bowel dysfunction improves quality of life, reduces incidence of urinary tract infection, and reduces health care costs. -
Ataxic Gait in Essential Tremor: a Disease-Associated Feature?
Freely available online Reviews Ataxic Gait in Essential Tremor: A Disease-Associated Feature? Ashwini K. Rao1* & Elan D. Louis2 1Department of Rehabilitation & Regenerative Medicine (Program in Physical Therapy), G.H. Sergievsky Center, Huntington's Disease Center of Excellence, Center of Excellence in Alzheimer's Disease, Columbia University, New York, NY, USA, 2Department of Neurology and Epidemiology (Chronic Diseases); Chief, Division of Movement Disorders, Co-Director- Center for Neuroepidemiology and Clinical Neurology Research, New Haven, CT, USA Abstract Background: While accumulating evidence suggests that balance and gait impairments are commonly seen in patients with essential tremor (ET), questions remain regarding their prevalence, their relationship with normal aging, whether they are similar to the impairments seen in spinocerebellar ataxias, their functional consequences, and whether some ET patients carry greater susceptibility. Methods: We conducted a literature search (until December 2018) on this topic. Results: We identified 23 articles on gait or balance impairments in ET. The prevalence of balance impairment (missteps on tandem walk test) was seven times higher in ET patients than controls. Gait impairments in ET included reduced speed, increased asymmetry, and impaired dynamic balance. While balance and gait problems worsened with age, ET patients were more impaired than controls, independent of age. The pattern of impairments seen in ET was qualitatively similar to that seen in spinocerebellar ataxias. Balance and gait impairments resulted in greater number of near falls in ET patients. Factors associated with balance and gait impairments in ET included age, presence of tremor in midline structures, and cognitive dysfunction. Discussion: Accumulating evidence suggests that balance and gait impairments are common in ET patients and occur to a greater extent in controls. -
Neurovascular Anatomy (1): Anterior Circulation Anatomy
Neurovascular Anatomy (1): Anterior Circulation Anatomy Natthapon Rattanathamsakul, MD. December 14th, 2017 Contents: Neurovascular Anatomy Arterial supply of the brain . Anterior circulation . Posterior circulation Arterial supply of the spinal cord Venous system of the brain Neurovascular Anatomy (1): Anatomy of the Anterior Circulation Carotid artery system Ophthalmic artery Arterial circle of Willis Arterial territories of the cerebrum Cerebral Vasculature • Anterior circulation: Internal carotid artery • Posterior circulation: Vertebrobasilar system • All originates at the arch of aorta Flemming KD, Jones LK. Mayo Clinic neurology board review: Basic science and psychiatry for initial certification. 2015 Common Carotid Artery • Carotid bifurcation at the level of C3-4 vertebra or superior border of thyroid cartilage External carotid artery Supply the head & neck, except for the brain the eyes Internal carotid artery • Supply the brain the eyes • Enter the skull via the carotid canal Netter FH. Atlas of human anatomy, 6th ed. 2014 Angiographic Correlation Uflacker R. Atlas of vascular anatomy: an angiographic approach, 2007 External Carotid Artery External carotid artery • Superior thyroid artery • Lingual artery • Facial artery • Ascending pharyngeal artery • Posterior auricular artery • Occipital artery • Maxillary artery • Superficial temporal artery • Middle meningeal artery – epidural hemorrhage Netter FH. Atlas of human anatomy, 6th ed. 2014 Middle meningeal artery Epidural hematoma http://www.jrlawfirm.com/library/subdural-epidural-hematoma -
The Alien Hand Syndrome: Classification of Forms Reported and Discussion of a New Condition
Neurol Sci (2003) 24:252–257 DOI 10.1007/s10072-003-0149-4 ORIGINAL F. Aboitiz • X. Carrasco • C. Schröter • D. Zaidel • E. Zaidel • M. Lavados The alien hand syndrome: classification of forms reported and discussion of a new condition Received: 24 February 2003 / Accepted in revised form: 14 June 2003 Abstract The term “alien hand” refers to a variety of clini- gories: (i) diagonistic dyspraxia and related syndromes, (ii) cal conditions whose common characteristic is the uncon- alien hand, (iii) way-ward hand and related syndromes, (iv) trolled behavior or the feeling of strangeness of one extremity, supernumerary hands and (v) agonistic dyspraxia. most commonly the left hand. A common classification distin- guishes between the posterior or sensory form of the alien Key words Alien hand • Agonistic dyspraxia • Corpus callo- hand, and the anterior or motor form of this condition. sum • Diagonistic dyspraxia • Frontal lobe • Parietal lobe • However, there are inconsistencies, such as the phenomenon Split brain of diagonistic dyspraxia, which is largely a motor syndrome despite being more frequently associated with posterior cal- losal lesions. We discuss critically the existing nomenclature and we also describe a case recently reported by us which does Introduction not fit any previously reported condition, termed agonistic dyspraxia. We propose that the cases of alien hand described A large variety of complex, abnormal, involuntary motor in the literature can be classified into at least five broad cate- behaviors have been described following callosal lesions which may or may not be accompained by hemispheric dam- age, especially in the frontal medial region. Although the dif- ferent terminologies used to describe these movements attempt to address their clinical specificity, there is a notice- F. -
Movement Disorders in Metabolic Disorders
Current Neurology and Neuroscience Reports (2019) 19: 7 https://doi.org/10.1007/s11910-019-0921-3 NEUROLOGY OF SYSTEMIC DISEASES (J BILLER, SECTION EDITOR) Movement Disorders in Metabolic Disorders José Luiz Pedroso1 & Orlando G. Barsottini1 & Alberto J. Espay2 Published online: 9 February 2019 # Springer Science+Business Media, LLC, part of Springer Nature 2019 Abstract Purpose of Review We provide a review of the movement disorders that complicate selected metabolic disorders, including the abnormal movements that may appear during or after their treatment. Recent Findings Movement disorders may be underrecognized when arising in the context of a broad range of metabolic disorders. Summary Abnormal movements may occur as the initial manifestation of a systemic disease, at any time during its course, or as a result of the medical interventions required for its management. Ascertaining movement phenome- nology in acute and subacute presentations may assist in the determination of the specific underlying metabolic disorder. The management of movement disorders associated with metabolic disorders depends on the underlying pathophysiology. Keywords Movement disorders . Abnormal movements . Metabolic disorders . Electrolytes . Internal medicine Introduction such as disorders of consciousness, headache, and sei- zures [3]. The metabolic origin can also be suspected Movement disorders such as parkinsonism, tremor, dys- when movement abnormalities appear in emergency set- tonia, chorea, and myoclonus most often arise in several tings or in intensive care units [4]. neurodegenerative or structural diseases of the basal Some common metabolic disorders, such as organ ganglia [1]. They may also be part of the clinical man- failure (particularly liver or renal insufficiency), endocri- ifestations of systemic metabolic disorders, as the initial nological diseases (e.g., hyperglycemia), and electrolyte feature, complicating its course, or as a result of the disturbances, are frequently present with neurological corrective treatment [2•]. -
Diagnosing Dementia: Signs, Symptoms and Meaning
Université de Montréal Diagnosing Dementia: Signs, Symptoms and Meaning Pa= Janice Elizabeth Graham Département d'anthropologie Faculté des arts et des sciences Thèse présentée à la Faculté des études supérieures en vue de l'obtention du grade de Philosophia Doctor 0h.D.) en anthropologie Janice E.Graharn, 1996 National Library Bibliothèque nationale I*I of Canada du Canada Acquisitions and Acquisitions et Bibtiographic Services services bibliographiques 395 Wellington Street 395, rue Wellington Ottawa ON K1A ON4 Ottawa ON KIA ON4 Canada Canada Vour fik Vorre réference Our file Notre refdrence The author has granted a non- L'auteur a accordé une licence non exclusive licence dowing the exdusive permettant à la National Library of Canada to Bibliothèque nationde du Canada de reproduce, loan, distribute or sell reproduire, prêter, distribuer ou copies of this thesis in microform, vendre des copies de cette thèse sous paper or electronic formats. la fome de microfiche/nlm, de reproduction sur papier ou sur format électroniq2e. The author retains ownership of the L'auteur conserve la propriété du copyright in this thesis. Neither the droit d'auteur qui protège cette thèse. thesis nor substantial extracts f?om it Ni la thèse ni des extraits substantiels may be printed or othenvise de celle-ci ne doivent être imprimés reproduced without the author's ou autrement reproduits sans son permission. autorisation. Université de Montréal Faculte des Btudes superieures Cette thèse ultitulee: Diagnosing Dementia: Signs, Symptoms and Meaning presentée -
Depression Prevalence in Postgraduate Students and Its Association with Gait Abnormality
SPECIAL SECTION ON DATA-ENABLED INTELLIGENCE FOR DIGITAL HEALTH Received November 7, 2019, accepted November 21, 2019, date of publication December 2, 2019, date of current version December 16, 2019. Digital Object Identifier 10.1109/ACCESS.2019.2957179 Depression Prevalence in Postgraduate Students and Its Association With Gait Abnormality JING FANG 1, TAO WANG 2, (Student Member, IEEE), CANCHENG LI 2, XIPING HU 1,2, (Member, IEEE), EDITH NGAI 3, (Senior Member, IEEE), BOON-CHONG SEET 4, (Senior Member, IEEE), JUN CHENG 1, YI GUO 5, AND XIN JIANG 6 1Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China 2School of Information Science and Engineering, Lanzhou University, Gansu 730000, China 3Department of Information Technology, Uppsala University, Uppsala 75105, Sweden 4Department of Electrical and Electronic Engineering, Auckland University of Technology, Auckland 1010, New Zealand 5Department of Neurology, Shenzhen People's Hospital, Second Clinical Medical College of Jinan University, First Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518020, China 6Department of Geriatrics, Shenzhen People's Hospital, Second Clinical Medical College of Jinan University, First Affiliated Hospital of Southern University of Science and Technology, Shenzhen 518020, China Corresponding authors: Xiping Hu ([email protected]) and Xin Jiang ([email protected]) This work was supported in part by Shenzhen Technology under Project JSGG20170413171746130, in part by the National Natural Science Foundation of China under Grant 61632014, Grant 61802159, Grant 61210010, Grant 61772508, and Grant 61402211, and in part by the Program of Beijing Municipal Science and Technology Commission under Grant Z171100000117005. ABSTRACT In recent years, an increasing number of university students are found to be at high risk of depression. -
TWITCH, JERK Or SPASM Movement Disorders Seen in Family Practice
TWITCH, JERK or SPASM Movement Disorders Seen in Family Practice J. Antonelle de Marcaida, M.D. Medical Director Chase Family Movement Disorders Center Hartford HealthCare Ayer Neuroscience Institute DEFINITION OF TERMS • Movement Disorders – neurological syndromes in which there is either an excess of movement or a paucity of voluntary and automatic movements, unrelated to weakness or spasticity • Hyperkinesias – excess of movements • Dyskinesias – unnatural movements • Abnormal Involuntary Movements – non-suppressible or only partially suppressible • Hypokinesia – decreased amplitude of movement • Bradykinesia – slowness of movement • Akinesia – loss of movement CLASSES OF MOVEMENTS • Automatic movements – learned motor behaviors performed without conscious effort, e.g. walking, speaking, swinging of arms while walking • Voluntary movements – intentional (planned or self-initiated) or externally triggered (in response to external stimulus, e.g. turn head toward loud noise, withdraw hand from hot stove) • Semi-voluntary/“unvoluntary” – induced by inner sensory stimulus (e.g. need to stretch body part or scratch an itch) or by an unwanted feeling or compulsion (e.g. compulsive touching, restless legs syndrome) • Involuntary movements – often non-suppressible (hemifacial spasms, myoclonus) or only partially suppressible (tremors, chorea, tics) HYPERKINESIAS: major categories • CHOREA • DYSTONIA • MYOCLONUS • TICS • TREMORS HYPERKINESIAS: subtypes Abdominal dyskinesias Jumpy stumps Akathisic movements Moving toes/fingers Asynergia/ataxia