Cricopharyngomyotomy As a Complimentary Procedure To
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Globus Hystericus — an Overview
Bangladesh Journal of Psychiatry. June, 1995, 7, 1, 32 GLOBUS HYSTERICUS — AN OVERVIEW Anwarul Haider1, M S I Mullick2, Md Shakhawat Islam3 Introduction Globus hystericus, Globus pharynges, Functional no abnormality7. The condition may be due to dysphagia, Globus syndrome are synonymous1. spasm of upper oesophageal sphincter. Many of It is a pscyhogenic disorder of alimentary tract the patients have reflux oesophagities. extremely common, the cause is poorly Oesphageal reflux due to abnormality in cardia understood, indeed may be relieved by may produce vague upper end symptoms, swallowing food or drink, occurs in tense anxious antacids reported to help if this is the case589. individuals23. Globus hystericus should not be diagnosed until an organic lesion especially a malignancy has been excluded10, all other causes of dysphagia Natural History : has to be excluded carefully. The patient often Persistent feeling or sensation of a lump in the admits to psychological stress or cancer phobia11. throat, usually in mid line, localised just above An attempt should be made to offer insight in the the supra steranl notch around the level of cricoid nature of the problem, a detail history, careful cartilage, is the commonest complain, mainly examination with x-ray if appropriate will help to occurs in anxious, middle aged, menopausal reassure a certain number of patients. A history ladies34. There is interference with swallowing but of friends or relatives with throat disease requires no true dysphagia for solid & liquid and the sympathetic probing12. symptoms often noticeable in empty swallowing One also has to remember that even most of saliva, are often diagnosed as globus if on neurotic patient, however on rare occasions is examination nothing found5. -
Peripheral Neuropathy in Complex Inherited Diseases: an Approach To
PERIPHERAL NEUROPATHY IN COMPLEX INHERITED DISEASES: AN APPROACH TO DIAGNOSIS Rossor AM1*, Carr AS1*, Devine H1, Chandrashekar H2, Pelayo-Negro AL1, Pareyson D3, Shy ME4, Scherer SS5, Reilly MM1. 1. MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology and National Hospital for Neurology and Neurosurgery, London, WC1N 3BG, UK. 2. Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, London, WC1N 3BG, UK. 3. Unit of Neurological Rare Diseases of Adulthood, Carlo Besta Neurological Institute IRCCS Foundation, Milan, Italy. 4. Department of Neurology, University of Iowa, 200 Hawkins Drive, Iowa City, IA 52242, USA 5. Department of Neurology, University of Pennsylvania, Philadelphia, PA 19014, USA. * These authors contributed equally to this work Corresponding author: Mary M Reilly Address: MRC Centre for Neuromuscular Diseases, 8-11 Queen Square, London, WC1N 3BG, UK. Email: [email protected] Telephone: 0044 (0) 203 456 7890 Word count: 4825 ABSTRACT Peripheral neuropathy is a common finding in patients with complex inherited neurological diseases and may be subclinical or a major component of the phenotype. This review aims to provide a clinical approach to the diagnosis of this complex group of patients by addressing key questions including the predominant neurological syndrome associated with the neuropathy e.g. spasticity, the type of neuropathy, and the other neurological and non- neurological features of the syndrome. Priority is given to the diagnosis of treatable conditions. Using this approach, we associated neuropathy with one of three major syndromic categories - 1) ataxia, 2) spasticity, and 3) global neurodevelopmental impairment. Syndromes that do not fall easily into one of these three categories can be grouped according to the predominant system involved in addition to the neuropathy e.g. -
Premature Loss of Permanent Teeth in Allgrove (4A) Syndrome in Two Related Families
Iran J Pediatr Case Report Mar 2010; Vol 20 (No 1), Pp:101-106 Premature Loss of Permanent Teeth in Allgrove (4A) Syndrome in Two Related Families Zahra Razavi*1, MD; MohammadMehdi Taghdiri¹, MD; Fatemeh Eghbalian¹, MD; Nooshin Bazzazi², MD 1. Department of Pediatrics, Hamadan University of Medical Sciences, IR Iran 2. Department of Ophthalmology, Hamadan University of Medical Sciences, IR Iran Received: Feb 07, 2009; Final Revision: Apr 27, 2009; Accepted: May 06, 2009 Abstract Background: Allgrove syndrome is a rare autosomal recessive condition characterized by adrenal insufficiency, achalasia, alacrima and occasionally autonomic disturbances. Mutations in the AAAS gene, on chromosome 12q13 have been implicated as a cause of this disorder. Case(s) Presentation: We present various manifestations of this syndrome in two related families each with two affected siblings in which several members had symptoms including reduced tear production, mild developmental delay, achalasia, neurological disturbances and also premature loss of permanent teeth in two of them, Conclusion: The importance of this report is dental involvement (loss of permanent teeth) in Allgrove syndrome that has not been reported in literature. Iranian Journal of Pediatrics, Volume 20 (Number 1), March 2010, Pages: 101106 Key Words: Achalasia, Adrenocortical Insufficiency, Alacrimia (Allgrove, triple‐A) Protein, Human; AAAS Protein, Human; Teeth; Allgrove Syndrome; Triple A Syndrome Protein, Human Introduction autonomic disturbances associated with Allgrove syndrome leading one author to In 1978 Allgrove and colleagues described 2 recommend the name 4A syndrome (adreno‐ unrelated pairs of siblings with achalasia and cortical insufficiency, achalasia of cardia, ACTH insensivity, three had impaired alacrima and autonomic abnormalities)[2‐4]. -
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Number 1 | January 2019 Prevalence and incidence of rare diseases: Bibliographic data Prevalence, incidence or number of published cases listed by diseases (in alphabetical order) www.orpha.net www.orphadata.org If a range of national data is available, the average is Methodology calculated to estimate the worldwide or European prevalence or incidence. When a range of data sources is available, the most Orphanet carries out a systematic survey of literature in recent data source that meets a certain number of quality order to estimate the prevalence and incidence of rare criteria is favoured (registries, meta-analyses, diseases. This study aims to collect new data regarding population-based studies, large cohorts studies). point prevalence, birth prevalence and incidence, and to update already published data according to new For congenital diseases, the prevalence is estimated, so scientific studies or other available data. that: Prevalence = birth prevalence x (patient life This data is presented in the following reports published expectancy/general population life expectancy). biannually: When only incidence data is documented, the prevalence is estimated when possible, so that : • Prevalence, incidence or number of published cases listed by diseases (in alphabetical order); Prevalence = incidence x disease mean duration. • Diseases listed by decreasing prevalence, incidence When neither prevalence nor incidence data is available, or number of published cases; which is the case for very rare diseases, the number of cases or families documented in the medical literature is Data collection provided. A number of different sources are used : Limitations of the study • Registries (RARECARE, EUROCAT, etc) ; The prevalence and incidence data presented in this report are only estimations and cannot be considered to • National/international health institutes and agencies be absolutely correct. -
French Clinical Practice Guidelines for Moyamoya Angiopathy
NEUROL-1879; No. of Pages 12 r e v u e n e u r o l o g i q u e x x x ( 2 0 1 8 ) x x x – x x x Available online at ScienceDirect www.sciencedirect.com Practice guidelines French clinical practice guidelines for Moyamoya angiopathy a, b c,1 d,1 D. Herve´ *, M. Kossorotoff , D. Bresson , T. Blauwblomme , e,1 f g h i M. Carneiro , E. Touze , F. Proust , I. Desguerre , S. Alamowitch , j k l m n J.-P. Bleton , A. Borsali , E. Brissaud , F. Brunelle , L. Calviere , o p q r M. Chevignard , G. Geffroy-Greco , S. Faesch , M.-O. Habert , s t a u v H. De Larocque , P. Meyer , S. Reyes , L. Thines , E. Tournier-Lasserve , a H. Chabriat a De´partement de neurologie, centre de re´fe´rence des maladies vasculaires rares du cerveau et de l’œil (CERVCO), groupe hospitalier Saint-Louis-Lariboisie`re-Fernand-Widal, 2, rue Ambroise-Pare´, 75010 Paris, France b Centre national de re´fe´rence de l’AVC de l’enfant, hoˆpital universitaire Necker-Enfants malades, AP–HP, 149, rue de Se`vres, 75015 Paris, France c Service de neurochirurgie, groupe hospitalier Saint-Louis-Lariboisie`re-Fernand-Widal, 2, rue Ambroise-Pare´, 75010 Paris, France d Service de neurochirurgie pe´diatrique, hoˆpital universitaire Necker–Enfants-Malades, AP–HP, 149, rue de Se`vres, 75015 Paris, France e Neurologie pe´diatrique, hoˆpital Femme-Me`re-Enfant, hospices Civils-de-Lyon, 59, boulevard Pinel, 69677 Bron, France f Service de neurologie, Normandie universite´, Unicaen, Inserm U1237, CHU Caen-Normandie, avenue de la Coˆte-de- Nacre, 14033 Caen, France g Service de neurochirurgie, -
Current Affairs Q&A
Current Affairs Q&A PDF This is Paid PDF provided by AffairsCloud.com, Our team is working hard in back end to provide quality PDF. If you not buy this paid PDF subscription plan, we kindly request you to buy pdf to avail this service. Help Us To Grow & Provide Quality Service Subscribe(Buy) Current Affairs PDF 2019 - Pocket, Study and Q&A (English & Hindi) Current Affairs Q&A PDF - September 2019 Table of Contents INDIAN AFFAIRS ................................................................................................................................................................................... 2 INTERNATIONAL AFFAIRS ............................................................................................................................................................ 59 BANKING & FINANCE ....................................................................................................................................................................... 87 ECONOMY & BUSINESS ................................................................................................................................................................. 112 AWARDS & RECOGNITIONS ........................................................................................................................................................ 128 APPOINTMENTS & RESIGNS ....................................................................................................................................................... 154 SCIENCE & TECHNOLOGY ........................................................................................................................................................... -
Orphanet Report Series Rare Diseases Collection
Marche des Maladies Rares – Alliance Maladies Rares Orphanet Report Series Rare Diseases collection DecemberOctober 2013 2009 List of rare diseases and synonyms Listed in alphabetical order www.orpha.net 20102206 Rare diseases listed in alphabetical order ORPHA ORPHA ORPHA Disease name Disease name Disease name Number Number Number 289157 1-alpha-hydroxylase deficiency 309127 3-hydroxyacyl-CoA dehydrogenase 228384 5q14.3 microdeletion syndrome deficiency 293948 1p21.3 microdeletion syndrome 314655 5q31.3 microdeletion syndrome 939 3-hydroxyisobutyric aciduria 1606 1p36 deletion syndrome 228415 5q35 microduplication syndrome 2616 3M syndrome 250989 1q21.1 microdeletion syndrome 96125 6p subtelomeric deletion syndrome 2616 3-M syndrome 250994 1q21.1 microduplication syndrome 251046 6p22 microdeletion syndrome 293843 3MC syndrome 250999 1q41q42 microdeletion syndrome 96125 6p25 microdeletion syndrome 6 3-methylcrotonylglycinuria 250999 1q41-q42 microdeletion syndrome 99135 6-phosphogluconate dehydrogenase 67046 3-methylglutaconic aciduria type 1 deficiency 238769 1q44 microdeletion syndrome 111 3-methylglutaconic aciduria type 2 13 6-pyruvoyl-tetrahydropterin synthase 976 2,8 dihydroxyadenine urolithiasis deficiency 67047 3-methylglutaconic aciduria type 3 869 2A syndrome 75857 6q terminal deletion 67048 3-methylglutaconic aciduria type 4 79154 2-aminoadipic 2-oxoadipic aciduria 171829 6q16 deletion syndrome 66634 3-methylglutaconic aciduria type 5 19 2-hydroxyglutaric acidemia 251056 6q25 microdeletion syndrome 352328 3-methylglutaconic -
Cricopharyngeal Myotomy Revisited
10.5005/jp-journals-10023-1019 Sudhakara M Rao et al CASE REPORT Cricopharyngeal Myotomy Revisited 1Sudhakara M Rao, 2Satishchandra T, 2PSN Murthy 1Associate Professor, Department of ENT and Head and Neck Surgery, Dr PSIMS and RF, Gannavaram, Andhra Pradesh, India 2Professor and Head, Department of ENT and Head and Neck Surgery, Dr PSIMS and RF, Gannavaram, Andhra Pradesh, India Correspondence: PSN Murthy, Professor and Head, Department of ENT and Head and Neck Surgery, Dr PSIMS and RF Gannavaram, Andhra Pradesh, India, e-mail: [email protected] ABSTRACT Dysphagia due to neuromuscular in coordination is major disability for the patient. Not able to swallow food or liquids inspite of healthy appetite makes the patient most irritable and can lead to psychological problems. Added to the swallowing problem patient also encounters symptoms and signs of laryngeal penetration or aspiration. For these patients, surgical option of cricopharyngeal myotomy offers a very good relief. We describe two cases where CP myotomy could facilitate a good swallow and prevent laryngeal stimulation or penetration and made a significant improvement in the quality of life of the patients. Keywords: Cricopharyngeal myotomy, Cricopharyngeal spasm, Neurogenic dysphasia, Cricopharyngeus muscle. INTRODUCTION myotomy in the same sitting under GA. He was given nasogastric feeds for 3 days before surgery. During surgery, hypo- Cricopharyngeal spasm can be a primary or secondary to several pharyngoscopy revealed no abnormality of postcricoid area. neurologic disorders.1 Mainly these are the patients who have a Another endotracheal tube was placed in the esophagus to identify basic neurologic disorder from which they were recovering but cricopharyngeal sphincter. -
Albany Med Conditions and Treatments
Albany Med Conditions Revised 3/28/2018 and Treatments - Pediatric Pediatric Allergy and Immunology Conditions Treated Services Offered Visit Web Page Allergic rhinitis Allergen immunotherapy Anaphylaxis Bee sting testing Asthma Drug allergy testing Bee/venom sensitivity Drug desensitization Chronic sinusitis Environmental allergen skin testing Contact dermatitis Exhaled nitric oxide measurement Drug allergies Food skin testing Eczema Immunoglobulin therapy management Eosinophilic esophagitis Latex skin testing Food allergies Local anesthetic skin testing Non-HIV immune deficiency disorders Nasal endoscopy Urticaria/angioedema Newborn immune screening evaluation Oral food and drug challenges Other specialty drug testing Patch testing Penicillin skin testing Pulmonary function testing Pediatric Bariatric Surgery Conditions Treated Services Offered Visit Web Page Diabetes Gastric restrictive procedures Heart disease risk Laparoscopic surgery Hypertension Malabsorptive procedures Restrictions in physical activities, such as walking Open surgery Sleep apnea Pre-assesment Pediatric Cardiothoracic Surgery Conditions Treated Services Offered Visit Web Page Aortic valve stenosis Atrial septal defect repair Atrial septal defect (ASD Cardiac catheterization Cardiomyopathies Coarctation of the aorta repair Coarctation of the aorta Congenital heart surgery Congenital obstructed vessels and valves Fetal echocardiography Fetal dysrhythmias Hypoplastic left heart repair Patent ductus arteriosus Patent ductus arteriosus ligation Pulmonary artery stenosis -
Management of Stroke in Neonates and Children: a Scientific Statement from the American Heart Association/American Stroke Association
UCSF UC San Francisco Previously Published Works Title Management of Stroke in Neonates and Children: A Scientific Statement From the American Heart Association/American Stroke Association. Permalink https://escholarship.org/uc/item/0sw5j7c1 Journal Stroke, 50(3) ISSN 0039-2499 Authors Ferriero, Donna M Fullerton, Heather J Bernard, Timothy J et al. Publication Date 2019-03-01 DOI 10.1161/str.0000000000000183 Peer reviewed eScholarship.org Powered by the California Digital Library University of California AHA/ASA Scientific Statement Management of Stroke in Neonates and Children A Scientific Statement From the American Heart Association/American Stroke Association The American Academy of Neurology affirms the value of this statement as an educational tool for neurologists. Donna M. Ferriero, MD, MS, FAHA, Co-Chair; Heather J. Fullerton, MD, MAS, Co-Chair; Timothy J. Bernard, MD, MSCS; Lori Billinghurst, MD, MSc, FRCPC; Stephen R. Daniels, MD, PhD; Michael R. DeBaun, MD, MPH; Gabrielle deVeber, MD; Rebecca N. Ichord, MD; Lori C. Jordan, MD, PhD, FAHA; Patricia Massicotte, MSc, MD, MHSc; Jennifer Meldau, MSN; E. Steve Roach, MD, FAHA; Edward R. Smith, MD; on behalf of the American Heart Association Stroke Council and Council on Cardiovascular and Stroke Nursing Purpose—Much has transpired since the last scientific statement on pediatric stroke was published 10 years ago. Although stroke has long been recognized as an adult health problem causing substantial morbidity and mortality, it is also an important cause of acquired brain injury in young patients, occurring most commonly in the neonate and throughout childhood. This scientific statement represents a synthesis of data and a consensus of the leading experts in childhood cardiovascular disease and stroke. -
With a Learning Disability; Guidance for General Practice
Improving identification of people with a learning disability: guidance for general practice NHS England and Improvement Publishing Approval Reference: 001030 Version 1 NHS England and NHS Improvement Contents Introduction .................................................................................... 2 Actions for practices ....................................................................... 4 Appendix 1: List of codes that indicate a learning disability ........... 7 Appendix 2: List of codes that may indicate a learning disability . 14 Appendix 3: List of outdated codes .............................................. 20 Appendix 4: Learning disability identification check-list ............... 22 1 | Contents Introduction 1. The NHS Long Term Plan1 commits to improve uptake of the existing annual health check in primary care for people aged over 14 years with a learning disability, so that at least 75% of those eligible have a learning disability health check each year. 2. There is also a need to increase the number of people receiving the annual seasonal flu vaccination, given the level of avoidable mortality associated with respiratory problems. 3. In 2017/18, only 44.6% of patients with a learning disability received a flu vaccination and only 55.1% of patients with a learning disability received an annual learning disability health check.2 4. In June 2019, NHS England and NHS Improvement announced a series of measures to improve coverage of annual health checks and flu vaccination for people with a learning disability. One of the commitments was to improve the quality of registers for people with a learning disability3. Clinical coding review 5. Most GP practices have developed a register of their patients known to have a learning disability. This has been developed from clinical diagnoses, from information gathered from learning disabilities teams and social services and has formed the basis of registers for people with learning disability developed for the Quality and Outcomes Framework (QOF). -
MBBS Syllabus
Syllabus BACHELOR OF MEDICINE AND BACHELOR OF SURGERY (MBBS) (4 ½ Years Degree Course + 1 Year Internship) 1/226 NOTICE 1. Amendments made by the Statutory Regulating Council i.e. Medical Council of India in Rules/ Regulations of Graduate Medical Courses shall automatically apply to the Rules/ Regulations of the Mahatma Gandhi University of Medical Sciences & Technology. 2. The University reserves the right to make changes in the syllabus/books/ guidelines, fee– structure or any other information at any time without prior notice. The decision of the University shall be binding on all. 3. The Jurisdiction of all court cases shall be Jaipur Bench of Hon'ble Rajasthan High Court only. 2/226 RULES & REGULATIONS OF BACHELOR OF MEDICINE & BACHELOR OF SURGERY (4½ Years Degree Course + 1 Year Internship) GOALS OF MEDICAL GRADUATE TRAINING PROGRAMME: (1) National Goals: At the end of undergraduate program, the medical student should be able to: (a) Recognize “health for all' as a national goal and right of all citizens and by undergoing training for medical profession, fulfil his/her social obligations towards realization of this goal. (b) Learn various aspects of National policies on health and devote him/her to its practical implementation. (c) Achieve competence in practice of holistic medicine, encompassing promotive, preventive, curative and rehabilitative aspects of common diseases (d) Develop scientific approach, acquire educational experience for proficiency in profession and promote healthy living. (e) Become exemplary citizen by observation