21. NINDS Forwarding Page Information sheet compiled by the National Institute of Neurological Disorders and Stroke. http://www.ninds.nih.gov/health_and_medical/disorders/kearns_sayre.htm

NINDS has redesigned its website and the URL for the page you were seeking has changed. The new URL for this page is /disorders/kearns_sayre/kearns_sayre.htm . Please update your bookmark to this page. You will be automatically taken to this page in 5 seconds, or you can click the link to go there now.

22. EMedicine - Chronic Progressive External Ophthalmoplegia : Article By Tracey A S kearnssayre syndrome (KSS) is a related mitochondrial myopathy that Ogasahara S, Nishikawa Y, Yorifuji S Treatment of kearns-sayre syndrome with http://www.emedicine.com/oph/topic510.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Ophthalmology Neurologic Disorders Chronic Progressive External Ophthalmoplegia Last Updated: August 5, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: CPEO, abiotrophic ophthalmoplegia, CPEO with ragged red fibers, oculocraniosomatic neuromuscular disease, ocular myopathy, Olson disease, Kearns-Sayre-Daroff syndrome, Kearns-Sayre syndrome, progressive external ophthalmoplegia plus, extraocular muscle paralysis AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Tracey A Schmucker, MD , Staff Physician, Department of Ophthalmology, University of Arkansas for Medical Sciences Coauthor(s): Hampton Roy, Sr, MD , Clinical Associate Professor, Department of Ophthalmology, University of Arkansas for Medical Sciences Editor(s): Edsel Ing, MD, FRCS(C)

23. Ryan's Hope Foundation Ryan McDonald is a 9 year old boy with kearnssayre syndrome. This site is to educate the public about Ryan and his struggle with this disorder, as well as raise funds for research to cure this disease. http://www.ryanshopefoundation.org

@import url(http://www.homestead.com/~media/elements/Text/font_styles.css); About Ryan... Ryan's Hope... A Cure for Kearns-Sayre Syndrome Ryan McDonald is a 9 year old boy from Michigan who has a degenerative disease called Kearns-Sayre Syndrome (KSS). KSS is an extremely rare, progressively fatal disease that affects the entire body. It is caused by a deletion in the mitochondrial DNA. Mitochondria are considered to be the "power houses" of the cells in our body. Their job is to convert the glucose from the food we eat into energy that can be utilized by the cell. The mitochondria know to do this because they have their own DNA, which differs from nuclear DNA, and to complicate matters, each cell in our body has anywhere from 1-500 mitochondria! The organs that require the most energy, therefore, have the most mitochondria are the brain, heart, eyes, and muscle tissue. These tissues are the most severely affected, resulting in progressive weakness until they are no longer able to function. KSS is a degenerative disease that is taking Ryan's cognitive intelligence, sight, hearing, and strength increasingly away.

24. Introduction: Kearns-Sayre Syndrome - WrongDiagnosis.com Introduction to kearnssayre syndrome as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis. http://www.wrongdiagnosis.com/k/kearns_sayre_syndrome/intro.htm

Home Symptoms Diseases Risks ... Diseases Search our medical database Subscribe to our free Newsletter sample Send this page to a friend Condition Lists By Organ By Symptom By Class By Prevalence ... List A-Z Current chapter: Kearns-Sayre Syndrome Next sections Basic Summary for Kearns-Sayre Syndrome Prevalence and Incidence of Kearns-Sayre Syndrome Symptoms of Kearns-Sayre Syndrome Treatments for Kearns-Sayre Syndrome ... Statistics about Kearns-Sayre Syndrome Next chapters: Progressive external ophthalmoplegia Myoclonus epilepsy MELAS Nutritional deficiency ... Feedback Introduction: Kearns-Sayre Syndrome Kearns-Sayre Syndrome: Rare mitochondrial muscle disorder. Kearns-Sayre Syndrome: Kearns-Sayre syndrome (KSS) is a rare neuromuscular disorder with onset usually before the age of 20. It is characterized by progressive external ophthalmoplegia (paralysis of the eye muscles) and mild skeletal muscle weakness. Researching symptoms of Kearns-Sayre Syndrome: Further information about the symptoms of Kearns-Sayre Syndrome is available including a list of symptoms of Kearns-Sayre Syndrome , or alternatively return to research other symptoms in the symptom center Treatments for Kearns-Sayre Syndrome: Various information is available about treatments available for Kearns-Sayre Syndrome , or research treatments for other diseases.

25. Basic Summary For Kearns-Sayre Syndrome - WrongDiagnosis.com Overview of kearnssayre syndrome as a medical condition including introduction, prevalence, prognosis, profile, symptoms, diagnosis, misdiagnosis, http://www.wrongdiagnosis.com/k/kearns_sayre_syndrome/basics.htm

Home Symptoms Diseases Risks ... Kearns-Sayre Syndrome Search our medical database Subscribe to our free Newsletter sample Send this page to a friend Condition Lists By Organ By Symptom By Class By Prevalence ... List A-Z Current chapter: Kearns-Sayre Syndrome Next sections Prevalence and Incidence of Kearns-Sayre Syndrome Symptoms of Kearns-Sayre Syndrome Treatments for Kearns-Sayre Syndrome Statistics about Kearns-Sayre Syndrome ... Statistics by Country for Kearns-Sayre Syndrome Next chapters: Progressive external ophthalmoplegia Myoclonus epilepsy MELAS Nutritional deficiency ... Feedback Basic Summary for Kearns-Sayre Syndrome Main name of condition: Kearns-Sayre Syndrome Other names or spellings: KSS What is Kearns-Sayre Syndrome? Brief description of Kearns-Sayre Syndrome: Rare mitochondrial muscle disorder. Parent types of Kearns-Sayre Syndrome: Mitochondrial diseases Organs Affected by Kearns-Sayre Syndrome: nerves muscles How many people get Kearns-Sayre Syndrome? Prevalance of Kearns-Sayre Syndrome: rare Who gets Kearns-Sayre Syndrome? Patient Profile for Kearns-Sayre Syndrome: Onset is usually before 20 What causes Kearns-Sayre Syndrome?

26. Kearns-Sayre Syndrome Information Page: National Institute Of Neurological Disor kearnssayre syndrome information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). http://www.ninds.nih.gov/disorders/kearns_sayre/kearns_sayre.htm

Accessible version Science for the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system More about Kearns-Sayre Syndrome Studies with patients Research literature Press releases Search NINDS... (help) Contact Us My Privacy NINDS is part of the National Institutes of Health You are here: Home Disorders Kearns-Sayre Syndrome NINDS Kearns-Sayre Syndrome Information Page Get Web page suited for printing Email this to a friend or colleague Table of Contents (click to jump to sections) What is Kearns-Sayre Syndrome? Is there any treatment? What is the prognosis? What research is being done? ... Organizations What is Kearns-Sayre Syndrome? Is there any treatment? Treatment for KSS is generally symptomatic and supportive. Cardiac abnormalities may be treated with various cardiac drugs or a pacemaker. What is the prognosis? The prognosis for individuals with KSS varies depending on the severity of symptoms. KSS is a slowly progressive disorder. What research is being done?

27. Kearns-Sayre Syndrome Links to articles, information, and resources for kearnssayre syndrome. http://rarediseases.about.com/cs/kearnssayresynd/

zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a70' About Rare / Orphan Diseases Rare Diseases Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Rare / Orphan Diseases newsletter! See Online Courses Search Rare / Orphan Diseases Kearns-Sayre Syndrome Guide picks A mitochondrial disorder that affects many body systems. Kearns Sayre Syndrome Article describes Kearns Sayre syndrome, its symptoms, diagnosis, and treatment. From the About.com Guide to Rare/Orphan Diseases. NORD: Kearns Sayre Syndrome Definition of the disorder from the National Organization for Rare Disorders (U.S.). MDC: Mitochonchondrial Myopathies Detailed information on mitochondrial myopathies from the Muscular Dystrophy Campaign (U.K.). MDA USA: Mitochondrial Myopathy References, clinical trials, and feature articles, from the Muscular Dystrophy Association (USA), on neuromuscular diseases caused by damage to mitochondria. NINDS: Mitochondrial Myopathies Information Page Information about mitochondrial myopathies such as Kearns Sayre syndrome.

28. Kearns-Sayre Syndrome Definition - Medical Dictionary Definitions Of Popular Med Online Medical Dictionary and glossary with medical definitions. http://www.medterms.com/script/main/art.asp?articlekey=30811

29. OMIM - KEARNS-SAYRE SYNDROME; KSS http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=530000

30. Entrez PubMed kearnssayre syndrome (KSS) is a mitochondrial disorder. There is a large-scale mitochondrial DNA (mtDNA) deletion in most of the case. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=9

31. Internet Scientific Publications, LLC. kearnssayre syndrome (KSS) is a very uncommon fatal multisystem disorder which usually Lestienne P, and Ponsot G. kearns-sayre syndrome with muscle http://www.ispub.com/ostia/index.php?xmlFilePath=journals/ijn/vol1n2/kss.xml

32. Eye Conditions > Kearns-Sayre Syndrome -- EyeMDLink.com kearnssayre syndrome. Chronic progressive external ophthalmoplegia (CPEO), also known as kearns-sayre syndrome, is a rare disorder, which is transmitted by http://www.eyemdlink.com/Condition.asp?ConditionID=259

33. HONselect - Kearns-Sayer Syndrome Kearnsayre Mitochondrial Cytopathy - kearns syndrome - kearns-sayre-Shy-Daroff Français, syndrome de kearns et sayre, - syndrome de kearns-sayre http://www.hon.ch/HONselect/RareDiseases/C05.651.460.700.500.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Kearns-Sayer Syndrome - Kearns Syndrome - Kearn-Sayre Mitochondrial Cytopathy - Kearns' Syndrome - Kearns-Sayre-Shy-Daroff Syndrome - Cytopathy, Kearn-Sayre Mitochondrial - Kearn Sayre Mitochondrial Cytopathy Français: Syndrome de Kearns et Sayre - Syndrome de Kearns-Sayre Deutsch: Kearns-Syndrom - Kearns-Sayre-Shy-Daroff-Syndrom - Kearns-Sayre-Syndrom Español: Síndrome de Kearns-Sayer - Síndrome de Kearns Português: Síndrome de Kearns-Sayer - Síndrome de Kearns HONselect ressources Definition: Yes Articles: Yes Images: Yes News: No Conferences: No Clinical trials: No Web sites: English No Français No Deutsch No Español No Português No Home About us Site map Search ... Contact http://www.hon.ch/HONselect/RareDiseases/C05.651.460.700.500.html Last modified: Wed May 18 2005

34. Syndrome De Kearns Et Sayre - Syndrome De Kearns-Sayre HONsélect Translate this page syndrome de kearns et sayre - articles, sites web, images, http://www.hon.ch/HONselect/RareDiseases/FR/C05.651.460.700.500.html

InitBulle("navy","#F8F8F8","#000066",1); sites HONcode sites Web HONsélect News ... Images Chercher HONsélect Anglais Français Allemand Espagnol Portugais le mot la partie du mot dans les termes MeSH Information pour "Syndrome de Kearns et Sayre": Hiérarchie médicale et definition Articles médicaux Ressources du Web Images médicales Nouvelles médicales Conférences médicales Hiérarchie Anglais Français Allemand Espagnol Portugais Syndrome de Kearns et Sayre Définition: A mitochondrial disorder featuring the triad of chronic progressive EXTERNAL OPHTHALMOPLEGIA , cardiomyopathy ( CARDIOMYOPATHIES ) with conduction block ( HEART BLOCK ), and RETINITIS PIGMENTOSA . Disease onset is in the first or second decade. Elevated CSF protein, sensorineural deafness, seizures, and pyramidal signs may also be present. Ragged-red fibers are found on muscle biopsy. (Adams et al., Principles of Neurology, 6th ed, p984) Synonyme(s): Syndrome de Kearns-Sayre / Voir connexe: Cardiomyopathies Ophtalmoplégie Rétinite pigmentaire Bloc cardiaque (NLM)® de l'INSERM (version française) Parcourir Chercher HONsélect Ressources du Web pour "Syndrome de Kearns et Sayre" Français Allemand = Site with HON description - = Site with a robot description info: entrez dans le site: (cliquez ci-dessous) domaine du site: HONcode - Syndrome de Kearns et Sayre : sites et documents francophones www.chu-rouen.fr

35. Kearns-Sayre Syndrome,KSS,Chronic Progressive External kearnssayre syndrome,KSS,Chronic Progressive External Ophthalmoplegia and Myopathy,CPEO with Myopathy,CPEO with Ragged-Red Fibers,KSS,Mitochondrial http://www.icomm.ca/geneinfo/kss.htm

36. Alpers Disease,Progressive Infantile Poliodystrophy,Barth Syndrome kearnssayre syndrome (KSS) Lactic Acidosis; Leber Hereditary Optic Neuropathy (LHON) Leigh s Disease (Subacute Necrotizing Encephalomyelopathy) http://www.icomm.ca/geneinfo/mitoch.htm

37. Kearns-Sayre Syndrome kearnssayre syndrome. DESCRIPTION Inherited disorder (autosomal dominant with onset before age 15). Characteristics - progressive ophthalmoplegia http://www.5mcc.com/Assets/SUMMARY/TP0500.html

Kearns-Sayre syndrome DESCRIPTION: Inherited disorder (autosomal dominant with onset before age 15). Characteristics - progressive ophthalmoplegia, pigmentary degeneration of the retina, ataxia, myopathy, cardiac conduction defect. Usual course - progressive; ophthalmic onset at ages 5-20; retinal onset at ages 8-40; cardiac onset at ages 10-40. CAUSES: unknown Synonyms: oculocraniosomatic neuromuscular disease ragged red fiber disease ophthalmoplegia-plus hereditary external ophthalmoplegia ICD-9-CM: 378.55 external ophthalmoplegia Author(s): Mark R. Dambro, MD Illustrations: Retinitis pigmentosa

38. CCHS Clinical Digital Library Miscellaneous kearnssayre syndrome Patient/Family Resources. The Family Village Library - Specific Diagnoses Card Catalog Table of contents http://cchs-dl.slis.ua.edu/patientinfo/metabolism/inborn/mitochondrial/kearns.ht

Patient/Family Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Patient/Family Resources Miscellaneous See also: Genetic Testing Patient/Family Resources General Genetic Disorders Patient/Family Resources General Metabolic Disorders Patient/Family Resources Kearns-Sayre Syndrome Clinical Resources National Institute of Neurological Disorders and Stroke: Homepage Disorders Information: List of documents Mitochondrial Myopathies: Access document Miscellaneous Kearns-Sayre Syndrome Patient/Family Resources The Family Village Library - Specific Diagnoses Card Catalog Table of contents Mitochondrial Disorders: Access document Healthfinder (US DHHS): Homepage Genetics: List of documents MedlinePlus (National Library of Medicine) Health Topics: Index Genetic Testing: List of documents Prenatal Testing: List of documents Genetic Counseling: List of documents Genetic Disorders: List of documents Birth Defects: List of documents YAHOO - Health:Diseases and Conditions:Metabolic Diseases Additional Metabolic Diseases resources ( These sites have not been reviewed.

39. CCHS Clinical Digital Library kearnssayre syndrome Access document. Pathology Resources. Kumar Robbins and Cotran Pathologic Basis of Disease 7th Ed.-2005 (MD Consult) Table of http://cchs-dl.slis.ua.edu/clinical/metabolism/inborn/mitochondrial/kearns.htm

Clinical Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Genetic Testing Clinical Resources General Genetic Disorders Clinical Resources General Metabolic Disorders Clinical Resources Kearns-Sayre Syndrome Patient/Family Resources Harrison's Principles of Internal Medicine 16th Ed.-2005: Table of contents Health Sciences Library subscription INFO Chapter 368. Muscular Dystrophies and Other Muscle Diseases: Table of contents Introduction: Access document Mitochondrial Myopathies: Access document Further Reading: Access document Goetz: Textbook of Clinical Neurology 2nd Ed.-2003 (MD Consult): Table of contents Health Sciences Library subscription INFO Chapter 31 - Aminoacidopathies and Organic Acidopathies, Mitochondrial Enzyme Defects, and Other Metabolic Errors: Access document Introduction: Access document Mitochondrial Enzyme Defects: Access document Reviews and Selected Updates: Access document References: Access document Zipes: Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine 7th Ed.-2005 (MD Consult):

40. Kearns-Sayre Syndrome (www.whonamedit.com) kearnssayre syndrome syndrome characterised by unilateral or bilateral progressive weakness of muscles of eyelids, up to severe ptosis, http://www.whonamedit.com/synd.cfm/1884.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. 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. A recommendation: Hypography is an open community about science and all things related Kearns-Sayre syndrome Also known as: Bernard-Scholz syndrome Kearns' syndrome Kearns-Shy syndrome Kearns-Sayre-Daroff syndrome Synonyms: 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. Associated persons: R. I. Barnard

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