Kearns Et Sayre, Syndrome : Arborescences MeSH Translate this page kearns et sayre, syndrome arborescences MeSH. kearns et sayre, syndrome C05.651.460.700.500 page PubMed du motclef page CISMeF du motclef http://www.chu-rouen.fr/navimesh/K/navikearnsetsayresyndrome.html
Extractions: Complete Atrioventricular Block in Kearns-Sayre Syndrome Universidade Federal Fluminense-UFF - Rio de Janeiro, RJ Arquivos Brasileiros de Cardiologia 67(2):, 1996 Full paper in portuguese A thirty-three year old woman, known to have Kearns-Sayre syndrome for eight years, had an ECG pattern of right bundle branch block and left anterior fascicular block that evolved to complete atrioventricular block, leading her to have a syncopal episode. A temporary pacemaker and then a permanent one were installed. The patient has been asymptomatic so far. Summary
Extractions: Fig. 3 1. Kearns TP, Sayre GP - Retinitis pigmentosa, external ophthalmoplegia and complete heart block. Arch Ophthalmol 1958; 60: 280. 2. Berenberg RA, Pellock JM, DiMauro S et al - Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome? Ann Neurol 1977; 1: 37-54. 3. Anan R, Nakagawa M, Miyata M et al - Cardiac involvement in mithocondrial diseases: a study on 17 patients with documented mithocondrial DNA defects. Circulation 1995; 91: 955-61. 4. Channer KS, Channer JL, Campbell MJ, Rees JR - Cardiomyopathy in the Kearns-Sayre syndrome. Br Heart J 1988; 59: 486-90. 5. Clark DS, Myerburg RJ, Morales AR, Befeler B, Hernandes FA, Gelband H - Heart block in Kearns-Sayre syndrome: electrophysiologic-pathologic correlation. Chest 1975; 68: 727-30. 6. Nitsch J, Zier S, Janssen KP et al - Indications for pacemaker therapy in ophthalmoplegia plus and Kearns-Sayre syndrome. Z Cardiol 1990; 79: 60-5.
Corneal Decompensation In A Boy With Kearns-Sayre Syndrome Corneal decompensation in a boy with kearnssayre syndrome. This paper describes the clinical history of a young boy with kearns-sayre syndrome. http://www.szp.swets.nl/szp/journals/og234247.htm
Extractions: 2002, Vol.23, No.4, pp. 247-251 Corneal decompensation in a boy with Kearns-Sayre syndrome F.N. Boonstra , I. Claerhout , F.A. Hol , G.P.A. Smit , van J.J.M. Collenburg and F.M. Meire Bartimeus Institute for Visually Handicapped Children, Zeist, The Netherlands University Medical Center, Department of Human Genetics, Nijmegen, The Netherlands University Hospital Groningen, Department of Pediatrics, Division of Metabolic Diseases, Groningen, The Netherlands Isala Klinieken, Department of Pediatrics, Zwolle, The Netherlands University Hospital of Ghent, Department of Ophthalmology, Belgium This paper describes the clinical history of a young boy with Kearns-Sayre syndrome. The first presenting symptom of Kearns-Sayre syndrome in this boy was corneal edema with photophobia and tearing.
Kears-Sayre Syndrome (www.whonamedit.com) Kearssayre syndrome syndrome characterised by unilateral or bilateral progressive Also known as Bernard-Scholz syndrome,kearns syndrome,kearns-Shy syndrome http://www.whonamedit.com/synd.cfm/1884.html
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. External ophthalmoplegia-retinitis pigmentosa-heart block syndrome, heart block-retinitis pigmentosa-ophthalmoplegia syndrome, oculocraniosomatic disease, oculo-cranio-somatic neuromuscular disease, oculopharingeal muscular dystrophy, ophthalmoplegia-pigmentary retinal degeneration-cardiomyopathy syndrome, ophthalmoplegia, ophthalmoplegia-retinal degeneration syndrome, and ophthalmoplegic retinal degeneration syndrome.
Blackwell Synergy - Cookie Absent Manometric study in kearnssayre syndrome. 1. Kapeller P, Fazekas F, Offenbacher Het al.kearns-sayre syndrome. Neurol Sciences 1996; 135 126-130. http://www.blackwell-synergy.com/links/doi/10.1111/j.1442-2050.2001.00152.x/abs/
Extractions: Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.
Blackwell Synergy - Cookie Absent Sustained Polymorphic Ventricular Tachycardia Unassociated with QT Prolongation or Bradycardia in the kearnssayre syndrome. kearns-sayre syndrome. http://www.blackwell-synergy.com/links/doi/10.1046/j.1460-9592.2003.00292.x/enha
Extractions: Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.
Endocrine Surgeon What is kearnssayre syndrome? This is a very rare syndrome and is also known as oculocraniosomatic disease. The main characteristics http://www.endocrinesurgeon.co.uk/pancreas/pancreas11-4.html
Extractions: Summaries of latest endocrine news......Up-to-date information at your fingertips...... Click on arrow to select.... Introduction to Endocrinology Thyroid Parathyroids Adrenals Pancreas Pituitary Multiple Endocrine Neoplasia Carcinoid tumours Erectile dysfunction Pineal Gland and Melatonin Osteoporosis Endocrine Anaesthetics A to Z of diagnostic tests Miscellaneous This is a very rare syndrome and is also known as oculocraniosomatic disease. The main characteristics of the syndrome are ophthalmoplegia and several endocrine abnormalities. One of the main endocrine abnormalities is diabetes mellitus as well as hypoparathyroidism and hypopituitarism. The cause and pathogenesis of the syndrome are not fully understood, but it is thought that there may be an important autoimmune component.
Karger Publishers Severe Hypomagnesemia and Hypoparathyroidism in kearnssayre syndrome KH Katsanos a , M. Elisaf a , E. Bairaktari b , EV Tsianos a a Department Internal http://content.karger.com/ProdukteDB/produkte.asp?Aktion=ShowAbstract&ProduktNr=
Extenza - Corneal Decompensation In A Boy With Kearns-Sayre Syndrome Corneal decompensation in a boy with kearnssayre syndrome. Keywords. corneal decompensation, kearns-sayre syndrome, child. Abstract text. http://www.extenza-eps.com/extenza/loadHTML?objectIDValue=13882&type=abstract
Disabilityexchange.org - Taxonomy kearnssayre syndrome. What is kearns-sayre syndrome? kearns-sayre syndrome (KSS) is a rare neuromuscular disorder with onset usually before the age of 20. http://www.disabilityexchange.org/taxonomy/index.php?fid=3&path=3_289
Kearns-Sayre Syndrom - Små Och Mindre Kända Handikappgrupper Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M. Progressive increase of the mutated mitochondrial DNA fraction in kearnssayre syndrome. http://www.sos.se/smkh/1999-29-090/1999-29-090.htm
Extractions: HTML-version 1.2 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. Orsak till sjukdomen/skadan Symtom centrala nervsystemet endokrina organ muskulaturen, Praktiska tips Resurspersoner Med dr Atle Melberg, Neurocentrum, Akademiska sjukhuset, 751 85 Uppsala, tel 018-616 30 00, fax 018-55 92 63.
Kearns-Sayre-Shy-Daroff Syndrome : On Medical Dictionary Online kearnssayre-Shy-Daroff syndrome defined on the Free Online Medical Dictionary. Link to the Medical Dictionary Online. kearns-sayre-Shy-Daroff syndrome. http://www.online-medical-dictionary.org/?q=Kearns-Sayre-Shy-Daroff Syndrome
Kearns Sayre Shy Daroff Syndrome : On Medical Dictionary Online kearns sayre Shy Daroff syndrome defined on the Free Online Medical Dictionary. Link to the Medical Dictionary Online. kearns sayre Shy Daroff syndrome. http://www.online-medical-dictionary.org/?q=Kearns Sayre Shy Daroff Syndrome
NINDS Kearns-Sayre Syndrome Information Page kearnssayre syndrome information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). What is kearns-sayre syndrome? http://accessible.ninds.nih.gov/health_and_medical/disorders/kearns_sayre.htm
Extractions: Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders-you are in this section ... Find People The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury Studies with patients Research literature Press release NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us NINDS Kearns-Sayre Syndrome Information Page Kearns-Sayre syndrome (KSS) is a rare neuromuscular disorder with onset usually before the age of 20. It is the result of abnormalities in the DNA of mitochondria - small rod-like structures found in every cell of the body that produce the energy that drives cellular functions. The mitochondrial diseases correlate with specific DNA mutations that cause problems with many of the organs and tissues in the body. KSS is characterized by progressive limitation of eye movements until there is complete immobility, accompanied by eyelid droop. It is also associated with abnormal accumulation of pigmented material on the membrane lining the eyes. Additional symptoms may include mild skeletal muscle weakness, heart block (a cardiac conduction defect), short stature, hearing loss, an inability to coordinate voluntary movements (ataxia), impaired cognitive function, and diabetes. Seizures are infrequent. Several endocrine disorders can be associated with KSS.
