Service Page - Pathologie Information DISEASE kearnssayre syndrome, CIM H49.8, The onset of kearns-sayresyndrome occurs before age 20. It is marked by ophthalmoplegia http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=480
ClinicalTrials.gov - Linking Patients To Medical Research Search Query Details. No studies were found for kearnssayre syndrome ALL-FIELDS.Modify Your Search. Individual Terms, Count. kearns-sayre syndrome , None. http://www.clinicaltrials.gov/search/term=Kearns-Sayre Syndrome
ClinicalTrials.gov - Linking Patients To Medical Research Search Query Details. No studies were found for NINDS kearnssayre syndrome InformationPage ALL-FIELDS. NINDS kearns-sayre syndrome Information Page , None. Page , 7. http://www.clinicaltrials.gov/search/term=NINDS Kearns-Sayre Syndrome Informatio
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.
Kearns Et Sayre, Syndrome : Sites Et Documents Francophones Translate this page kearns Et sayre, syndrome. Menu général CISMeF. Arborescence(s) du thesaurusMeSH contenant le mot-clé kearns et sayre, syndrome kearns syndrome http://www.chu-rouen.fr/ssf/pathol/kearnsetsayresyndrome.html
Kearns Et Sayre, Syndrome : Arborescences MeSH Translate this page kearns Et sayre, syndrome. kearns et sayre, syndrome C05.651.460.700.500 pageCISMeF du motclef système nerveux, maladies C10 page CISMeF du motclef http://www.chu-rouen.fr/navimesh/navikearnsetsayresyndrome.html
Provision Of Educationally-related Servi... Translate this page Titre/Title, Journal of Child Neurology. Article, kearns-sayre syndrome with a novelmitochondrial DNA deletion. Identification, Aug., no 8 15 2000 Pages 555-57. http://www.cidg.com/~marienf/k/i/n/m017180.htm
Extractions: # Article : A0031581 Cote/Call Number Auteur/Author American Academy of Pediatrics. Committee on children with disabilities. Titre/Title Pediatrics Article Provision of educationally-related services for children and adolescents with chronic disease and disabling conditions. (RE9929) Identification Feb., No 2 105 2000 Pages: 448-51 Descripteurs/Descriptors Enfant malade chronique Demande par
Provision Of Related Services For Childr... Translate this page Cote/Call Number, WD205/Mitchondr. Auteur/Author, Titre/Title, Article,kearns-sayre, syndrome de. Identification, 2000 Pages 2 p. Descripteurs http://www.cidg.com/~marienf/k/i/n/m017179.htm
Extractions: # Article : A0031580 Cote/Call Number Auteur/Author American Academy of Pediatrics. Committee on children with disabilities. Titre/Title Pediatrics Article Provision of related services for children with chronic disabilities. (RE9339) Identification Dec., o 6 92 1993 Pages: 879-81 Descripteurs/Descriptors Demande par
Extractions: MoI = Mode of Inheritance: a: autosomal, ad: autosomal dominant, ar: autosomal recessive, xl: x-linked, mt: mitochondrial References Attree,O., Olivos,I.M., Okabe,I., Bailey,L.C., Nelson,D.L., Lewis,R.A., McInnes,R.R., and Nussbaum,R.L. The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase. 1992; Nature. 358: 239-242.
Kearns-Sayre Syndrome The Official Parent's Sourcebook on kearnssayre syndrome (Chronic ProgressiveExternal Ophthalmoplegia and Myopathy; Chronic Progressive External http://www.icongrouponline.com/health/Kearns_Sayre.html
Extractions: (Chronic Progressive External Ophthalmoplegia and Myopathy; Chronic Progressive External Ophthalmoplegia with Ragged Red Fibers; hereditary external ophthalmoplegia; Kearns-Sayre Disease; Mitochondrial Cytopathy, Kearn-Sayre Type; oculocraniosomatic neuromuscular disease; Oculocraniosomatic Syndrome (obsolete); Ophthalmoplegia Plus Syndrome; Ophthalmoplegia, Pigmentary Degeneration of the Retina and Cadiomyopathy; ophthalmoplegia-plus; ragged red fiber disease) Revised and Updated for the Internet Age Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Electronic File * E-Book version sent via e-mail in 2 business days Electronic File * E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Kearns Sayre. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Chronic Progressive External Ophthalmoplegia and Myopathy; Chronic Progressive External Ophthalmoplegia with Ragged Red Fibers; hereditary external ophthalmoplegia; Kearns-Sayre Disease; Mitochondrial Cytopathy, Kearn-Sayre Type; oculocraniosomatic neuromuscular disease; Oculocraniosomatic Syndrome (obsolete); Ophthalmoplegia Plus Syndrome; Ophthalmoplegia, Pigmentary Degeneration of the Retina and Cadiomyopathy; ophthalmoplegia-plus; ragged red fiber disease
Kears-Sayre Syndrome (www.whonamedit.com) Kearssayre syndrome syndrome characterised by unilateral or bilateral progressive Alsoknown as Bernard-Scholz syndrome,kearns' syndrome,kearns-Shy syndrome http://www.whonamedit.com/synd.cfm/1884.html
Extractions: 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. Syndrome characterised by unilateral or bilateral progressive weakness of muscles of eyelids, up to severe ptosis, pigmentary degeneration of retina, cardiomegaly/cardiomyopathy, and heart failure. Some cases present cerebellar ataxia, progressive paralysis, sensory deafness for high tones, spasticity, mental deficiency, and short stature. Prevalent in females. Onset before 20 years of age. The syndrome is sometimes classified into an infantile and a juvenile form. Both sexes affected. Aetiology unknown. Sporadic and familial forms known. Autosomal dominant inheritance has been suggested in some cases. First described jointly by Kearns and Sayre in 1958. The combination of ophthalmoplegia and pigment degeneration had been described earlier by Barnard and Scholz in 1944, Chamlin and Billet in 1950, Erdbrink 1957, etc. In 1946 the British neurologist Paul Sandifer reported ophthalmoplegia and cardiomyopathy.
Endocrine Surgeon What is kearnssayre syndrome? This is a very rare syndrome and is alsoknown 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.
Endocrine Surgeon K. kearnssayre syndrome. http://www.endocrinesurgeon.co.uk/conditionindex/k.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 K
Ophthalmoplegia kearnssayre syndrome causes ophthalmoplegia along with loss of pigmentin the retina, the light-sensitive membrane lining the eye. http://www.healthatoz.com/healthatoz/Atoz/ency/ophthalmoplegia.html
Extractions: Definition Ophthalmoplegia is a paralysis or weakness of one or more of the muscles that control eye movement. The condition can be caused by any of several neurologic disorders. It may be myopathic, meaning that the muscles controlling eye movement are directly involved, or neurogenic, meaning that the nerve pathways controlling eye muscles are affected. Diseases associated with ophthalmoplegia are ocular myopathy, which affects muscles, and internuclear ophthalmoplegia, a disorder caused by multiple sclerosis , a disease which affects nerves. Description Because the eyes do not move together in ophthalmoplegia, patients may complain of double vision. Double vision is especially troublesome if the ophthalmoplegia comes on suddenly or affects each eye differently. Because ophthalmoplegia is caused by another, underlying disease, it is often associated with other neurologic symptoms, including limb weakness, lack of coordination, and numbness. Causes and symptoms Ocular myopathy is also known as mitochondrial encephalomyelopathy with ophthalmoplegia or progressive external ophthalmoplegia. Because it is so often associated with diseases affecting many levels of the neurologic system, it is often referred to as "ophthalmoplegia plus." The main feature is progressive limitation of eye movements, usually with drooping of the eyelids (
