Re: Kearns-Sayre Syndrome neuromuscular diseases message board. Re kearnssayre syndrome. In Reply to kearns-sayre syndrome posted by Julie on January 08, 2000 at 080300 http://www.healthboards.com/neuromuscular-diseases/410.html
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ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page Version pour Impression, MALADIE kearns-sayre, syndrome de, CIM H49.8, Quelques rares syndromes de Pearson ont évolué vers un syndrome de kearns-sayre. http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=480
ORPHANET - Rare Diseases - Orphan Drugs Printing version, DISEASE kearnssayre syndrome, ICD H49.8, The onset of kearns-sayre syndrome occurs before age 20. It is marked http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=480
Cardiomyopathy In The Kearns-Sayre Syndrome. Cardiomyopathy in the kearnssayre syndrome. Channer KS, Channer JL, Campbell MJ, Rees JR. Department of Cardiology, Bristol Royal Infirmary. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=DocSum
CCHS Clinical Digital Library Clinical Resources by Topic Metabolic Disorders. kearnssayre syndrome Clinical Resources. kearns-sayre syndrome Access document. http://cchs-dl.slis.ua.edu/clinical/metabolism/inborn/mitochondrial/kearns.htm
Extractions: Clinical Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: Chapter 67: Diseases Caused by Genetic Defects of Mitochondria: Table of contents Goetz: Textbook of Clinical Neurology 2nd Ed.-2003 (MD Consult):
Extractions: Patient/Family Resources by Topic: Metabolic Disorders Kearns-Sayre Syndrome Patient/Family Resources Miscellaneous See also: Miscellaneous Kearns-Sayre Syndrome Patient/Family Resources Healthfinder (US DHHS): Homepage National Library of Medicine MEDLINE plus Health Topics: Index YAHOO - Health:Diseases and Conditions:Metabolic Diseases
Kearns-Sayre Syndrome Information Diseases Database kearnssayre syndrome may cause or feature Medical information linkskearns-sayre syndrome specific sites. Medical dictionary, library and http://www.diseasesdatabase.com/ddb7137.htm
Extractions: Kearns-Sayre Syndrome,KSS,Chronic Progressive External Ophthalmoplegia and Myopathy,CPEO with Myopathy,CPEO with Ragged-Red Fibers,KSS,Mitochondrial Cytopathy Kearn-Sayre Type,Oculocraniosomatic Syndrome (obsolete),Ophthalmoplegia,Pigmentary Degeneration of the Retina and Cadiomyopathy,Kearns-Sayre Disease,Chronic Progressive External Ophthalmoplegia with Ragged Red Fibers,Ophthalmoplegia Plus Syndrome Kearns-Sayre Syndrome is a rare neuromuscular disorder characterized by three primary findings: progressive paralysis of certain eye muscles (chronic progressive external ophthalmoplegia [CPEO]); abnormal accumulation of colored (pigmented) material on the nerve-rich membrane lining the eyes (atypical retinitis pigmentosa), leading to chronic inflammation, progressive degeneration, and wearing away of certain eye structures (pigmentary degeneration of the retina); and heart disease (cardiomyopathy) such as heart block.
Kearns-Sayre Syndrome Ailment Name kearnssayre syndrome. Join this Community get help by emailing and chatting to others, and sharing information and experiences, http://www.thirdaid.com/conditions/Kearns-Sayre_Syndrome.htm
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KEARNS-SAYRE SYNDROME Features Listed For kearnssayre syndrome. McKusick 165100. Cardiomyopathy; Deafness, conductive; Deafness, sensorineural; ECG abnormality/conduction defects; http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?914
Kearns-Sayre Syndrome kearnssayre syndrome PubMed Medline search on kearns-sayre syndrome Mitochondrial myopathies factsheet National Institute for http://www.ion.ucl.ac.uk/library/patient/kearnes.htm
World Of Ophthalmology - Kearns Syndrome Other Links. ? About.com kearnssayre syndrome ? eMedicine kearns-sayre syndrome Medical Textbooks for Health Professionals and Consumers. http://wmed.narod.ru/w_ophth/diseases/e_hrd/hr_14.htm
Extractions: W Dr. Victor Zamyatin's Personal Web Site Ophthalmology - Home Page Anatomy Physiology Diseases Diagnostic Tests Surgical Procedures Medications Journals ... Index Encyclopaedia of Ophthalmology - Greatest Links' Collection Greatest Medical Journals' Collection Catalogue of Ophthalmological Journals Online Journal of World Ophthalmological Events Catalogue of Opthalmic Images ... Retinitis Pigmentosa Kearns Syndrome MeSH description A mitochondrial disorder featuring the triad of chronic progressive external ophthalmoplegia, cardiomyopathy (with conduction 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)
Kearns-Sayre Syndrome Medical Wisdom kearnssayre syndrome Information Page. Table of Contents (click to jump to sections). What is kearns-sayre syndrome? Is there any treatment? http://medicalwisdom.com/health/disorders/kearns_sayre.htm
Extractions: 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. Is there any treatment?
Entrez PubMed Mitochondrial cytopathy (kearnssayre syndrome) Article in Serbian Jovicic A, Ivanisevic V, Spasic P, Vujicic M. Vojnomedicinska akademija, Institut za http://www.biomedcentral.com/pubmed/2343566
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Kearns-Sayre Syndrome » Medical Diagnosis Medical Diagnosis » K » kearnssayre syndrome. kearns-sayre syndrome. kearns-sayre syndrome. OVERVIEW Inherited disorder (autosomal http://www.medfamily.org/diagnosis/K/diagnosis-terms-Kearns_Sayre_syndrome.phtml
Extractions: Z Kearns-Sayre syndrome 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. 378.55 external ophthalmoplegia Although the medFamily materials have been developed by physicians and health care provider it is designed for educational purposes only. The site is not engaged in rendering medical advice. The information provided should not be used for diagnosing or treating a health problem or a disease. It is not a substitute for professional care. It is solely for information and second opinion purposes. If you have or suspect you may have a health problem, you should consult your health care provider and use the information here as a cross references. The authors, editors, producers, sponsors, and contributors shall have no liability, obligation or responsibility to any person or entity for any loss, damage, or adverse consequence alleged to have happened directly or indirectly as a consequence of this material.
Extractions: 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. Although the medFamily materials have been developed by physicians and health care provider it is designed for educational purposes only. The site is not engaged in rendering medical advice. The information provided should not be used for diagnosing or treating a health problem or a disease. It is not a substitute for professional care. It is solely for information and second opinion purposes. If you have or suspect you may have a health problem, you should consult your health care provider and use the information here as a cross references. The authors, editors, producers, sponsors, and contributors shall have no liability, obligation or responsibility to any person or entity for any loss, damage, or adverse consequence alleged to have happened directly or indirectly as a consequence of this material.
Mitochondrial Disorders kearnssayre syndrome. Infancy Low birth weight; Death; Metabolic lactic acidosis; May precede development of kearns-sayre syndrome if survival past infancy. http://www.neuro.wustl.edu/neuromuscular/mitosyn.html
Kearns Et Sayre, Syndrome : Sites Et Documents Francophones Translate this page kearns et sayre, syndrome. Menu général CISMeF. Arborescence(s) du thesaurus MeSH contenant le mot-clé kearns et sayre, syndrome kearns syndrome http://www.chu-rouen.fr/ssf/pathol/kearnsetsayresyndrome.html
Extractions: Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; description et signes de la maladie, sites internet, dysmorphologie, conseil génétique, neurologie pédiatrique, maladies métaboliques, neuromusculaires et neurométaboliques, diagnostic pré-symptomatique de myologie et cardiomyopathie, laboratoires de diagnostic, projets de recherche en cours, associations de patients ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2002 ; visité le : 27/10/2003].
