SLCentral Directory - Health - Conditions And Diseases - M 4); Marfan Syndrome@ (37); MarieSainton Disease@ (4); marinesco-sjogren syndrome@ (5); Master s Disease@ (4); Mayer Rokitansky Kuster http://www.slcentral.com/directory/index.php/Health/Conditions_and_Diseases/M/
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Useful Links Marfan Syndrome National Marfan Foundation http//www.marfan.org/; marinescosjogren syndrome Support Website http//www.marinesco-sjogren.org; http://www.genetichealthvic.net.au/pages/links.html
Extractions: Home Better Health Channel - http://www.betterhealth.vic.gov.au/ Department of Human Services - http://www.dhs.vic.gov.au/ GENZYME Therapeutics - http://www.genzyme.com.au/ Haemscreen - http://haemscreen.com/ Health On Line - http://www.health.abol.net.au/ Health Insurance Commission - http://www.hic.gov.au/ McMillan Shakespeare - http://www.mcms.com.au/ Medical Practitioners Board Of Victoria - http://www.mpbofv.org.au/ Monash Medical Centre - http://www.southernhealth.org.au/ Murdoch Childrens Research Institute - http://murdoch.rch.unimelb.edu.au/ OMIM: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM Possum - http://www.possum.net.au/ Royal Children's Hospital - http://www.rch.unimelb.edu.au/ Royal Women's Hospital - http://www.rch.unimelb.edu.au/index-ext.html Southern Health - http://www.southernhealth.org.au/ Specimen Collection - http://www.rch.unimelb.edu.au/lab services/specimen.collection.xls
M In Health > Conditions And Diseases 4); Marfan Syndrome@ (37); MarieSainton Disease@ (4); marinesco-sjogren syndrome@ (5); Master s Disease@ (3); Mayer Rokitansky Kuster http://ilectric.com/glance/Health/Conditions_and_Diseases/M/
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Extractions: The UMDF Medical Article List Subject: Oxidative Phosphorylation Back to the Subject List United Mitochondrial Disease Foundation We welcome any suggested additions to our list. Last updated: 26-Jun-98 REFERENCE FORMAT: Author Lastname; Firstname; Article Number; Article Title; Journal or Book; Year; Volume; Page Numbers Bentlage ; H ; 605* ; Human diseases with defects in oxidative phosphorylation. 1. Decreased amounts of assembled oxidative phosphorylation complexes in mitochondrial encephalomyopathies. ; 1995 ; 227(3) ; 909-15 Berio ; A ; 3202 hem ; Marinesco-Sjogren syndrome with chronic progressive ophthalmoplegia caused by presumed defective oxidative phosphorylation ; Pediatr Med Chir ; 1996 ; 18(1) ; 99-103 Bioulac-Sage ; P ; 847 ; Fatal neonatal liver failure and mitochondrial cytopathy (oxidative phosphorylation deficiency): a light and electron microscopic study of the liver. ; Hepatology ; 1993 ; 18(4) ; 839-46 Casta ; A ; 5758 ; Perioperative white matter degeneration and death in a patient with a defect in mitochondrial oxidative phosphorylation. ; Anesthesiology ; 1997 ; 87(2) ; 420-5
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Extractions: mesothelioma cancer 1 to 10 of 10 results. Up One Level Topia!: Health: Support Groups: Conditions and Diseases: Cancer (99) Bone Marrow Transplant (topiasearch) Brain and CNS@ (21) Breast (topiasearch) Gastrointestinal@ (0) Genitourinary@ (0) Hematologic@ (0) Lung (topiasearch) Skin (topiasearch) See Also: Health: Conditions and Diseases: Cancer Cancer Message Board - Non-monitored message board. Vital Options - TeleSupport Cancer Networt.Innovative radio talk show, The Group Room. The Group Room uses communi Up One Level Topia!: Health: Conditions and Diseases: Cancer: Mesothelioma (14) See Also: Health: Conditions and Diseases: Respiratory Conditions: Asbestosis Health: Occupational Health and Safety: Hazardous Substances: Asbestos Society: Law: Legal Information: Product Liability: Occupational: Asbestos Virtual Hospital: Mesothelioma - Information on pleural mesotheliomas, including clinical presentation, diagnosis, treatment, pathology and case studies. From the University o Up One Level Topia!: Health: Conditions and Diseases: Cancer (1594) AIDS Related (topiasearch) Brain and CNS (topiasearch) Breast (topiasearch) Carcinoid (topiasearch) Centers (topiasearch) Coping (topiasearch) Endocrine (topiasearch) Eye (topiasearch) Gastrointestinal (topiasearch) Genitourinary (topiasearch) Gynecologic (topiasearch) Head and Neck (topiasearch) Hematologic (topiasearch) Journals (topiasearch) Lung (topiasearch) Melanoma (topiasearch) Mesothelioma (topias
Baylor Neurology Case Of The Month Hartnup disease, juvenile GM2 gangliosidosis, juvenile sulfatide lipidosis, maple syrup urine disease, marinescosjogren syndrome, Refsum disease, pyruvate http://www.bcm.tmc.edu/neurol/challeng/pat25/summary.html
Extractions: Diagnosis: Friedreich's Ataxia Patient #25 presented with progressive gait and limb ataxia, mild distal symmetrical sensory loss, dimished deep tendon reflexes, weakness of the gluteal muscles, and bilateral extensor plantar responses. These findings indicate cerebellar, peripheral nerve (or dorsal root ganglion), and corticospinal involvement and imply a multisystem degenerative disease. There was no evidence of autonomic dysfunction, and eye movements were left unaffected. Extrapyramidal involvement was not present arguing against one of the Multi-System Atrophies (MSAs), such as olivopontocerebellar atrophy (OPCA). The most salient feature in this case is the patient's marked progressive ataxia. Ataxia may be due either to cerebellar or proprioceptive dysfunction, though it is rarely difficult to distinguish the two. However, when both are present, diagnostic difficulties arise. The findings in this case - gait and limb ataxia, titubation, loss of check response, and dysdiadochokinesia - point to an abnormality in the cerebellar system. This patient also had evidence of a peripheral neuropathy with involvement of the posterior columns evidenced by decreased position and vibratory sense. The degree of proprioceptive abnormality was not sufficient to explain the marked gait disturbance, however. While this patient exhibited dysfunction in both the cerebellar and proprioceptive systems, the cerebellar involvement was most impressive. The primary defect, therefore lies somewhere in the connections to, from, or within the cerebellum.
NR Workshop 2000 Cases 2, 11, ?, , marinescosjogren syndrome. 2, 12, , , Wilson disease(subgroup; pseudosclerosis). http://nrws2000.umin.ac.jp/cases.html
Marinesco-Sjogren-Garland Syndrome Information Diseases Database marinescosjogren-Garland syndrome Cataract-oligophrenia syndrome, Disease Database Information marinesco-sjogren-Garland syndrome Definition(s) via UMLS ..Code translations and terms via UMLS http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=31430
Marinesco-Sjögren Syndrome Support Group Website http//www.marinescosjogren.org. E-mail marinesco-sjogren@pacbell.net. Conditions Marinesco-Sjögren syndrome http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Mari
ORPHANET® : Marinesco-Sjogren, Syndrome De Translate this page ORPHANET. Accès à la base de données Orphanet. marinesco-sjogren, syndrome de. Accès direct aux détails Résumé Le syndrome de http://www.orpha.net/static/FR/marinescosjogren.html
Extractions: Le syndrome de Marinesco-Sjögren associe une cataracte congénitale, un retard psycho-moteur et une ataxie cérébelleuse. Les muscles squelettiques présentent une atrophie d'origine neurogène, une dégénérescence vacuolaire et une augmentation de la variabilité du calibre des fibres musculaires. Il est vraisemblable qu'il s'agisse d'une maladie lysosomale bien que l'anomalie enzymatique n'ait pas encore été identifiée. En cas de suspicion clinique, l'examen d'une biopsie conjonctive peut permettre de révéler une augmentation très nette du nombre des lysosomes dans les fibroblastes. Il semble que les patients aient une concentration sérique basse de vitamine E et une absence de chylomicrons en période post-prandiale. Ce syndrome est transmis sur un mode récessif autosomique. *Auteur : Dr S. Aymé (septembre 2002)*. Signes de la maladie Mise à jour : 01/06/2004 Accès à la base de données Orphanet
ORPHANET - Maladies Rares - Médicaments Orphelins Translate this page Version pour Impression, MALADIE marinesco-sjogren, syndrome de, CIM E88.9, Le syndrome de Marinesco-Sjögren associe une cataracte http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=559
Extractions: Cataract-oligophrenia syndrome Marinesco-Sjogren-Garland syndrome: Definition(s) via UMLS Code translations and terms via UMLS Marinesco-Sjogren-Garland syndrome: specific sites Send Marinesco-Sjogren-Garland syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these:
Marinesco Sjogren Syndrome Marinesco Sjogren syndrome Important It is possible that the main title of the report Marinesco Sjogren syndrome is not the name you expected. http://my.webmd.com/hw/health_guide_atoz/nord868.asp
Extractions: Marinesco-Sjogren Syndrome is a rare disorder that is inherited through autosomal recessive genes. The major features of this disorder are a loss of muscle coordination as a result of disease in the cerebellum (cerebellar ataxia), loss of clearness in the eyes' lenses (cataract), increased muscle tension (spasticity), progressive muscle weakness, and mental deficiency.
Index Marden Walker syndrome Mareo Marfan syndrome Marfanoid Hypermobility syndrome Marie Disease MarieSainton Disease Marinesco Sjogren syndrome Marinesco-Garland http://my.webmd.com/hw/index/index-topics-M.asp
Health Library Marcus Gunn Phenomenon. Marden Walker syndrome. Marfan syndrome. Marinesco Sjogren syndrome. Maroteaux Lamy syndrome. Marshall Smith syndrome. Marshall syndrome. http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/_SearchResul
Health Library - Marinesco Sjogren syndrome. Important It is possible that the main title of the report Marinesco Sjogren syndrome is not the name you expected. http://12.31.13.29/library/healthguide/IllnessConditions/topic.asp?hwid=nord868
Marinesco Sjogren Syndrome: A Case Report. Marinesco Sjogren syndrome a case report. Neurology India. ABSTRACT Three members of one family suffering from Marinesco Sjogren syndrome are being reported. http://medind.nic.in/imvw/imvw10178.html
Extractions: Extracted from IndMED Surekha RK; Panagaria A; Sharma D Department of Neurolgy, SMS Medical College, Jaipur, India. Marinesco Sjogren syndrome: a case report. Neurology India. 1997 Mar; 45(1): 28-30 ABSTRACT: Three members of one family suffering from Marinesco Sjogren syndrome are being reported. All the three cases had mental retardation, congenital bilateral cataracts and cerebellar ataxia. It is a rare autosomal recessive disorder. KEYWORDS: Spinocerebellar Degeneration/GE; Spinocerebellar Degeneration/CN; Mental Retardation/GE; Cataract/GE; Cerebellar Ataxia/GE; Case Report; Human; Male; Female; Adult Record Identifier: NM000387