A Dictionary of Neurological Signs
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Brain Death and the Cervical Spinal Cord: a Confounding Factor for the Clinical Examination
Spinal Cord (2010) 48, 2–9 & 2010 International Spinal Cord Society All rights reserved 1362-4393/10 $32.00 www.nature.com/sc REVIEW Brain death and the cervical spinal cord: a confounding factor for the clinical examination AR Joffe, N Anton and J Blackwood Department of Pediatrics, Stollery Children’s Hospital, University of Alberta, Edmonton, Alberta, Canada Study design: This study is a systematic review. Objectives: Brain death (BD) is a clinical diagnosis, made by documenting absent brainstem functions, including unresponsive coma and apnea. Cervical spinal cord dysfunction would confound clinical diagnosis of BD. Our objective was to determine whether cervical spinal cord dysfunction is common in BD. Methods: A case of BD showing cervical cord compression on magnetic resonance imaging prompted a literature review from 1965 to 2008 for any reports of cervical spinal cord injury associated with brain herniation or BD. Results: A total of 12 cases of brain herniation in meningitis occurred shortly after a lumbar puncture with acute respiratory arrest and quadriplegia. In total, nine cases of acute brain herniation from various non-meningitis causes resulted in acute quadriplegia. The cases suggest that direct compression of the cervical spinal cord, or the anterior spinal arteries during cerebellar tonsillar herniation cause ischemic injury to the cord. No case series of brain herniation specifically mentioned spinal cord injury, but many survivors had severe disability including spastic limbs. Only two pathological series of BD examined the spinal cord; 56–100% of cases had upper cervical spinal cord damage, suggesting infarction from direct compression of the cord or its arterial blood supply. -
Cryptococcal Meningoencephalitis with Fulminant Intracranial Hypertension: an Unexpected Cause of Brain Death
Case Report Singapore Med J 2010; 51(8) : e133 Cryptococcal meningoencephalitis with fulminant intracranial hypertension: an unexpected cause of brain death Teo Y K ABSTRACT and later developed fulminant cryptococcal The diagnosis of brain death requires the meningoencephalitis, leading to brain death. presence of unresponsiveness and a lack of receptivity, the absence of movement, CASE REPORT breathing and brain stem reflexes, as well as A 61-year-old Caucasian man presented with a two-week a state of coma in which the cause has been history of generalised malaise, loss of appetite, nausea, identified. We report a case of brain death that headache and unsteady gait with frequent falls. The was diagnosed based on clinical neurological patient was initially seen at a local hospital, where a non- examinations, and supported by the absence contrast computed tomography (CT) of the brain did not of cerebral blood flow on magnetic resonance reveal any abnormality. He was treated symptomatically angiography and electroencephalography with oral analgesics. The patient had end-stage renal demonstrating the characteristic absence failure secondary to hypertension and had undergone of electrical activity. Thorough clinical an autologous renal transplant from his wife one year examination and repeated imaging of the ago. The patient was on prednisolone 10 mg once a brain revealed no apparent clinical cause or day, tacrolimus 3 mg twice a day and mycophenolate mechanism of brain death. We proceeded (mofetil) 1 g twice a day for immunosuppression. He with organ donation of the deceased’s liver had persistent symptoms, as described above and was and corneas. However, postmortem revealed admitted to a tertiary hospital for further evaluation. -
The Epidemiology of the Cerebral Palsies
Clinics in Developmental Medicine No. 87 The Epidemiology of the Cerebral Palsies Edited by FIONA STANLEY EVA ALBERMAN 1984 Spastics International Medical Publications OXFORD: Blackwell Scientific Publications Ltd. PHILADELPHIA: J. B. Lippincott Co. CHAPTER 11 Prenatal and Perinatal Risk Factors in a Survey of 681 Swedish Cases BENGT and GUDRUN HAGBERG I, that am curtail'd of this fair proportion, Cheated of feature by dissembling nature, , Deform'd, unfinish'd, sent before my time Into this breathing world, scarce half made up, And that so lamely and unfashionable That dogs bark at me, as I halt by them. Shakespeare, Richard III Introduction The aim of this chapter is to try and shed light on more specific aspects of the main groups of prenatal causes and risk factors for cerebral palsy, their mutual importance, and particularly their relationship to superimposed detrimental perinatal events. This survey is based on an investigation of 681 cases born in Sweden from 1959 to 1976. In our original retrospective analysis of causes of cerebral palsy (Hagberg et al. 1975a), it was found necessary to make certain generalisations about the aetiological groupings. Only the risk factor that was considered to be the predominating possible cause was used for classification. There is no doubt that this oversimplifies the issue as it neglects the complex network of different interacting detrimental risk factors that are present in the majority of cases, and in all probability underlie the development of brain lesions. Definitions For the purpose of the Swedish investigation, the following definition of cerebral palsy was used: a non-progressive 'disorder of movement and posture due to a defect or lesion of the immature brain' (Bax 1964). -
Approach to a Case of Congenital Heart Disease
BAI JERBAI WADIA HOSPITAL FOR CHILDREN PEDIATRIC CLINICS FOR POST GRADUATES PREFACE This book is a compilation of the discussions carried out at the course for post-graduates on ” Clinical Practical Pediatrics” at the Bai Jerbai Wadia Hospital for Children, Mumbai. It has been prepared by the teaching faculty of the course and will be a ready-reckoner for the exam-going participants. This manual covers the most commonly asked cases in Pediatric Practical examinations in our country and we hope that it will help the students in their practical examinations. An appropriately taken history, properly elicited clinical signs, logical diagnosis with the differential diagnosis and sound management principles definitely give the examiner the feeling that the candidate is fit to be a consultant of tomorrow. Wishing you all the very best for your forthcoming examinations. Dr.N.C.Joshi Dr.S.S.Prabhu Program Directors. FOREWARD I am very happy to say that the hospital has taken an initiative to organize this CME for the postgraduate students. The hospital is completing 75 years of its existence and has 2 done marvelous work in providing excellent sevices to the children belonging to the poor society of Mumbai and the country. The hospital gets cases referred from all over the country and I am proud to say that the referrals has stood the confidence imposed on the hospital and its faculty. We do get even the rarest of the rare cases which get diagnosed and treated. I am sure all of you will be immensely benefited by this programme. Wish you all the best in your examination and career. -
Radiculopathy Vs. Spinal Stenosis: Evocative Electrodiagnosis Identifies the Main Pain Generator
Functional Electromyography Loren M. Fishman · Allen N. Wilkins Functional Electromyography Provocative Maneuvers in Electrodiagnosis 123 Loren M. Fishman, MD Allen N. Wilkins, MD College of Physicians & Surgeons Manhattan Physical Medicine Columbia University and Rehabilitation New York, NY 10028, USA New York, NY 10013, USA [email protected] ISBN 978-1-60761-019-9 e-ISBN 978-1-60761-020-5 DOI 10.1007/978-1-60761-020-5 Springer New York Dordrecht Heidelberg London Library of Congress Control Number: 2010935087 © Springer Science+Business Media, LLC 2011 All rights reserved. This work may not be translated or copied in whole or in part without the written permission of the publisher (Springer Science+Business Media, LLC, 233 Spring Street, New York, NY 10013, USA), except for brief excerpts in connection with reviews or scholarly analysis. Use in connection with any form of information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed is forbidden. The use in this publication of trade names, trademarks, service marks, and similar terms, even if they are not identified as such, is not to be taken as an expression of opinion as to whether or not they are subject to proprietary rights. While the advice and information in this book are believed to be true and accurate at the date of going to press, neither the authors nor the editors nor the publisher can accept any legal responsibility for any errors or omissions that may be made. The publisher makes no warranty, express or implied, with respect to the material contained herein. -
Basilar Artery and Its Branches Called Pontine Arteries
3 Farah Mohammad Ahmad Al-Tarefe Mohammad Al salem تذكر أ َّن : أولئك الذين بداخلهم شيء يفوق كل الظروف ، هم فقط من استطاعوا أ ّن يحققوا انجازاً رائعاً .... كن ذا همة Recommendation: Study this sheet after you finish the whole anatomy material . Dr.Alsalem started talking about the blood supply for brain and spinal cord which are mentioned in sheet#5 so that we didn't write them . 26:00-56:27/ Rec.Lab#3 Let start : Medulla oblengata : we will study the blood supply in two levels . A- Close medulla (central canal) : It is divided into four regions ; medial , anteromedial , posteriolateral and posterior region. Medially : anterior spinal artery. Anteromedial: vertebral artery posterolateral : posterior inferior cerebellar artery ( PICA). Posterior : posterior spinal artery which is a branch from PICA. B-Open medulla ( 4th ventricle ) : It is divided into four regions ; medial , anteromedial , posteriolateral region. Medially : anterior spinal artery. Anteromedial: vertebral artery posterolateral : posterior inferior cerebellar artery ( PICA). 1 | P a g e Lesions: 1- Medial medullary syndrome (Dejerine syndrome): It is caused by a lesion in anterior spinal artery which supplies the area close to the mid line. Symptoms: (keep your eyes on right pic). Contralateral hemiparesis= weakness: the pyramid will be affected . Contralateral loss of proprioception , fine touch and vibration (medial lemniscus). Deviation of the tongue to the ipsilateral side when it is protruded (hypoglossal root or nucleus injury). This syndrome is characterized by Alternating hemiplegia MRI from Open Medulla (notice the 4th ventricle) Note :The Alternating hemiplegia means ; 1- The upper and lower limbs are paralyzed in the contralateral side of lesion = upper motor neuron lesion . -
Analysis of Fourteen New Cases of Meningovascular Syphilis: Renewed Interest in an Old Problem
Open Access Original Article DOI: 10.7759/cureus.16951 Analysis of Fourteen New Cases of Meningovascular Syphilis: Renewed Interest in an Old Problem Faiza Aziouaz 1 , Fatima Zahra Mabrouki 2 , Mohammed Chraa 3 , Nisrine Louhab 3 , Nawal Adali 3 , Imane Hajjaj 3 , Najib Kissani 3 , Yassine Mebrouk 1 1. Neurology, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Oujda, MAR 2. Ophthalmology, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Oujda, MAR 3. Neurology, Faculty of Medicine and Pharmacy, Mohammed VI University Hospital, Marrakech, MAR Corresponding author: Faiza Aziouaz, [email protected] Abstract Neurosyphilis (NS) remains a public health problem. Several recent reports suggest a worldwide increase in the incidence of this condition. Various syndromes can occur in NS, such as syphilitic meningitis, meningovascular syphilis, parenchymatous and gummatous neurosyphilis. Syphilis meningovascular will be the focus of this study. We report 14 new observations of meningovascular syphilis. A review of demographic and clinical features, neuroimaging findings, cerebrospinal fluid changes, treatment and outcome, pathophysiology mechanism of meningovascular syphilis are presented. Categories: Neurology, HIV/AIDS, Infectious Disease Keywords: neurosyphilis, stroke, vasculitis, csf, acquired immune deficiency syndrome (aids) Introduction The incidence of stroke is approximately 2.3/1000/year, based on community surveys [1]. Stroke can be a complication of a central nervous system infection [2]. Some infections are more often associated with cerebrovascular complications than others, and the pathogenesis of vascular lesions varies widely from one disease to another [2, 3]. Most of these conditions cause stroke through a mechanism of angitis [4]. This review focuses on meningovascular syphilis as an infectious cause of stroke. -
Alternating Hemiplegia of Childhood Syndrome
orphananesthesia Anaesthesia recommendations for Alternating Hemiplegia of Childhood syndrome Disease name: Alternating hemiplegia of childhood syndrome (AHC) ICD 10: G98 Synonyms: AHC syndrome (An ATP1A3-related neurologic disorder). AHC was named for its most striking and diagnostic motor symptom; however, the range of manifestations show it to be a CNS disorder affecting function broadly in various brain circuits, heart and the disease evolves with age. Disease summary: AHC is a very rare neurological disorder first described in 1971 which has received increasing interest recently [1]. It is characterized by hemiplegia of either side of the body, paroxysmal tonic or dystonic spells, oculomotor abnormalities and developmental delay.2-4 Onset occurs before 18 months of age. This condition is diagnosed based on the occurrence of the above combination of symptoms, is usually due to de novo pathogenic variant in ATP1A3 and has also been reported in a few families [2-3]. Onset and progression of neurological symptoms have been well characterized. While the course and severity of deficits can vary considerably, there appears to be progression over time, at least in some patients. The differential diagnosis of AHC includes familial hemiplegic migraine (FHM) syndromes (e.g. FHM1-CACNA1A; FHM2-ATP1A2), episodic ataxia type 6, glutamate transporter disorders (SLC1A3), glucose transporter defects, GLUT1 deficiency (SLC2A1), infantile onset epileptic encephalopathies, severe myoclonic epilepsy of infancy (Dravet syn- drome), SCN1A mutations, mitochondrial disorders, and disorders of dopamine biosynthesis/ neurotransmitter disorders. The prevalence has been estimated at 1:1,000,000 with most cases being due to de novo mutations [4-6]. Triggers in AHC and other ATP1A3 related diseases that can induce paroxysmal episodes in AHC are frequent. -
Synesthetes: a Handbook
Synesthetes: a handbook by Sean A. Day i © 2016 Sean A. Day All pictures and diagrams used in this publication are either in public domain or are the property of Sean A. Day ii Dedications To the following: Susanne Michaela Wiesner Midori Ming-Mei Cameo Myrdene Anderson and subscribers to the Synesthesia List, past and present iii Table of Contents Chapter 1: Introduction – What is synesthesia? ................................................... 1 Definition......................................................................................................... 1 The Synesthesia ListSM .................................................................................... 3 What causes synesthesia? ................................................................................ 4 What are the characteristics of synesthesia? .................................................... 6 On synesthesia being “abnormal” and ineffable ............................................ 11 Chapter 2: What is the full range of possibilities of types of synesthesia? ........ 13 How many different types of synesthesia are there? ..................................... 13 Can synesthesia be two-way? ........................................................................ 22 What is the ratio of synesthetes to non-synesthetes? ..................................... 22 What is the age of onset for congenital synesthesia? ..................................... 23 Chapter 3: From graphemes ............................................................................... 25 -
Foreign Accent Syndrome, a Rare Presentation of Schizophrenia in a 34-Year-Old African American Female: a Case Report and Literature Review
Hindawi Publishing Corporation Case Reports in Psychiatry Volume 2016, Article ID 8073572, 5 pages http://dx.doi.org/10.1155/2016/8073572 Case Report Foreign Accent Syndrome, a Rare Presentation of Schizophrenia in a 34-Year-Old African American Female: A Case Report and Literature Review Kenneth Asogwa,1 Carolina Nisenoff,1 and Jerome Okudo2 1 Richmond University Medical Center, 355 Bard Avenue, Staten Island, NY 10310, USA 2University of Texas School of Public Health, 1200 Pressler Street, Houston, TX 77030, USA Correspondence should be addressed to Jerome Okudo; [email protected] Received 17 October 2015; Revised 14 December 2015; Accepted 29 December 2015 AcademicEditor:ErikJonsson¨ Copyright © 2016 Kenneth Asogwa et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Foreign Accent Syndrome (FAS) is a rare phenomenon where speech is characterized by a new accent to the patient’snative language. More than 100 cases with the syndrome have been published, the majority of which were associated with observed insults of the speech center. Some other cases have been described without identifiable organic brain injury, especially in patients with psychiatric illness. This paper presents a patient with schizophrenia and FAS, without any evidence of organic brain injury. FAS recurred during psychotic exacerbation and did not reverse before transfer to a long-term psychiatric facility. The case is discussed in the context of a brief review of the syndrome. 1. Introduction had a history of paranoid schizophrenia. The patient was brought to the psychiatry emergency room by ambulance Foreign Accent Syndrome (FAS) is a rare condition where for evaluation of aggression. -
Cerebral Palsy the ABC's of CP
Cerebral Palsy The ABC’s of CP Toni Benton, M.D. Continuum of Care Project UNM HSC School of Medicine April 20, 2006 Cerebral Palsy Outline I. Definition II. Incidence, Epidemiology and Distribution III. Etiology IV. Types V. Medical Management VI. Psychosocial Issues VII. Aging Cerebral Palsy-Definition Cerebral palsy is a symptom complex, (not a disease) that has multiple etiologies. CP is a disorder of tone, posture or movement due to a lesion in the developing brain. Lesion results in paralysis, weakness, incoordination or abnormal movement Not contagious, no cure. It is static, but it symptoms may change with maturation Cerebral Palsy Brain damage Occurs during developmental period Motor dysfunction Not Curable Non-progressive (static) Any regression or deterioration of motor or intellectual skills should prompt a search for a degenerative disease Therapy can help improve function Cerebral Palsy There are 2 major types of CP, depending on location of lesions: Pyramidal (Spastic) Extrapyramidal There is overlap of both symptoms and anatomic lesions. The pyramidal system carries the signal for muscle contraction. The extrapyramidal system provides regulatory influences on that contraction. Cerebral Palsy Types of brain damage Bleeding Brain malformation Trauma to brain Lack of oxygen Infection Toxins Unknown Epidemiology The overall prevalence of cerebral palsy ranges from 1.5 to 2.5 per 1000 live births. The overall prevalence of CP has remained stable since the 1960’s. Speculations that the increased survival of the VLBW preemies would cause a rise in the prevalence of CP have proven wrong. Likewise the expected decrease in CP as a result of C-section and fetal monitoring has not happened. -
The Interpretation Ofdysprosody in Patients with Parkinson's Disease 147 J Neurol Neurosurg Psychiatry: First Published As 10.1136/Jnnp.54.2.145 on 1 February 1991
Journal ofNeurology, Neurosurgery, and Psychiatry 1991;54:145-148 145 The interpretation of dysprosody in patients with J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.54.2.145 on 1 February 1991. Downloaded from Parkinson's disease J F V Caekebeke, A Jennekens-Schinkel, M E van der Linden, 0 J S Buruma, R A C Roos Abstract functions4 has not been resolved. It would Prosodic features in the speech pro- even have implications for a revision of duction of 21 patients with idiopathic current theories on the relation between Parkinson's disease were tested. The cerebral dysfunction and disorders of emotion appreciation of vocal and facial expres- or affect. The right and left cerebral hemi- sion was also examined in the same spheres have both been suggested as the patients. Significant intergroup differ- representational locus of prosody,9 with an ences were found in the prosody produc- intrahemispheric distribution of dysprosodia tion tasks but, in contrast to previous subtypes reflecting the aphasias.'0 results, not in the receptive tasks on the The aims of the study were: (a) to verify recognition and appreciation of prosody dysprosody in a controlled replication study and of facial expression. The discrepancy of patients with PD; (b) to explore relations between the production and recognition between dysprosody and cognitive, affective of prosodic features does not support the and perceptual variables in the same patients. suggestion that dysprosody in Parkin- son's disease is necessarily a disorder of' processing emotional information that Subjects and methods could be misinterpreted as a dysarthria. Subjects Twenty one PD patients attending the outpatients clinic and 14 control subjects This study concerns "dysprosody" and its participated after giving informed consent.