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         Marinesco-sjogren Syndrome:     more detail

61. Health Library
Marcus Gunn Phenomenon. Marden Walker syndrome. Marfan syndrome. Marinesco Sjogrensyndrome. Maroteaux Lamy syndrome. Marshall Smith syndrome. Marshall syndrome.
http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/_SearchResults.

62. Short Description Of Cell Lines. Pathology: Marinesco-Sjogren Syndrome *248800
Version 4.200205, Short description of cell lines. Pathology MarinescoSjogrensyndrome *248800 OMIM record. - By selecting the cell
http://www.biotech.ist.unige.it/cldb/pat112.html
Version
Short description of cell lines.
Pathology: Marinesco-Sjogren syndrome
OMIM record
By selecting the cell line name , you will receive the detailed description of the cell line
By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines
You can search any term of the list by using the 'Find' utility of your browser
human, Caucasian
skin, fibroblast GEIMM
By Beatrice...

63. Rare Musculoskeletal Disorders.
Conradi Hunermann syndrome. Marinesco Sjogren syndrome. Split Hand Deformity
http://www.orthoknow.com/support/rare-disorders.htm
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Gordon Syndrome Proteus Syndrome ... Top

64. NORD - National Organization For Rare Disorders, Inc.
Marinesco Sjogren syndrome. To purchase fulltext report ($7.50) Copyright 1992,1995 Synonyms of Marinesco Sjogren syndrome Marinesco-Garland syndrome;
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Marinesco Sjo

65. Untitled Document
Ataxia cerebellaria Marinesco Sjogren syndrome Epilepsy SjögrenLarsson-syndromeMental retardation Marinesco Sjogren syndrome Addison's disease DOOR syndrome
http://home.tiscali.nl/sb137765/d.cns.html
Ataxia cerebellaria Marinesco Sjogren Syndrome Epilepsy Mental retardation Marinesco Sjogren Syndrome Addison's disease DOOR syndrome Vitamine-B12-deficiency ... De-Sanctis-Cacchione-Syndrome Microcephaly De-Sanctis-Cacchione-Syndrome Neuropathy lower limbs Amyloidosis hereditaria Paralysis spasticdiplegia or quadriplegia speech defects thalamus etc angiomatosis Bonnet-Dechaume-Blanc-Syndrome Psychiatrical Causes Acne-Excoriatum Alopecia Ataxia-Teleangiectasia Cheilitis-Factitia Cladosporiosis brain absces skin nodu De-Sanctis-Cacchione-Syndrome Decubitus-Ulcers Delusions-Hallucinations Depressions Dermatitis-seborrhoic Emotions-And-Dermatoses Epilepsy Erythema-E-pudore Facial-Palsy Farber's-Disease Glossodynia Hypochondria Lipogranuloma-Penis-Scrotum Lyme-Disease Mental-Retardation Meralgia-Paraesthetica Moynahan-Syndrome Parkinson-Syndrome Sweat-Gland-Necrosis Syphilis-IV Trichotillomania Trisomy-13 Trisomy-18-Edwards-Syndrome XYY-Syndrome

66. Untitled Document
Cacchionesyndrome Ellis-VanCrefeld-syndrome Erythroderma-Ichthyosiformis GargoylismMac-Kusick-syndrome Marinesco Sjogren syndrome Osteodysplastic-Geroderma
http://home.tiscali.nl/sb137765/diagnosis.symptoms1.html
Achondroplasia Osteogenesis-Imperfecta Acromegaly Acromegaly Adrenal virilism syndrom e Calcinosis-Metasticum ... XXXXY-Syndrome Ankylosis Acanthosis Nigricans Dracunculosis Psoriasis-Arthropathica Werner-Syndrome Arachnodactily Marfan S arm radio ulnar synostosis Klinefelter-Syndrome a rms-and-legs-short Conradi-Syndrome Ellis-VanCrefeld-Syndrome Osteogenesis-Imperfecta Vinyl-Chloride-Disease Arms hypoplasia radius en fibula Seckel-Syndrome Arthralgia see also Arthritis Acne-fulminans Blastomycosis Cold-Urticaria Familial-Mediteranean-Fever Hepatitis-A-Virus Hepatitis-B-Virus Lipoatrophia-Semicircularis Lyme-Disease Mixed-Connective-Tissue-Syndrome Panniculitis-Nodosa Periarteritis-nodosa-cutanea Polyarteritis-Nodosa Schistosomiasis-Visceral Serum-Sickness Sickle-Cell-Anemia SLE-Arthritis Sweet-Syndrome Syphilis-II-Macular Urticaria-DrugInduced Vasculitis-Cutanea Bird face prominent nose narrow Dysostosis-Mandibulofacialis Goltz-Syndrome Hallermann-Streiff-Syndrome Rothmund-Thomson-Syndrome Seckel-Syndrome Bone pain - macroglobuliemia Bones tall Marfan Syndrome brachydactylie fingers short andstubby Mal de Meleda Nail-Patella-Syndrome Oro-Facial-Digital-syndromes Racket-Nail Rubinstein-Taybi-Syndrome Silver-Syndrome Conradi-Syndrome Tricho-Rhino-Phalangeal-Syndrom brachycephaly boad skull Apert syndrome campodactylia bent fingers 3.4.5.

67. Birth Disorder Information Directory - J
Arthritis List of Sites. Juvenile Cataract with Cerebellar Atrophy,Myopathy and Mental Retardation (Marinesco Sjogren Like syndrome)
http://www.bdid.com/defectj.htm

HOME
J
Jabs Houk Bias Syndrome (Blau Syndrome, Blau Type Arthrocutaneouveal Granulomatosis, Synovitis Granulomatous Uveitis Cranial Neuropathies) Jackson Barr Syndrome (Deafness Conductive Ptosis Skeletal Anomalies) Jackson Weiss Syndrome (Craniosynostosis Midfacial Hypoplasia Foot Abnormalities; Acrocephalosyndactyly, Jackson Weiss Type) Jacobs Syndrome Jacobsen Syndrome (JBS; Deletion/Distal/Monosomy 11q[-] (Syndrome, Partial); Partial Monosomy of Long Arm of Chromosome 11) Jadassohn Lewandowsky Syndrome (Circumscribed Disseminated Keratosis Jadassohn Lewandowsky Type, Pachyonychia Congenita with Natal Teeth [Type I]) Jadassohn Nevus Phakomatosis Jaffe Campanacci Syndrome (Fibromatosis Multiple Non Ossifying) Jaffer Beighton Syndrome (Marfanoid Build Spondylolisthesis Constricted Pelvis) Jagell Holmgren Hofer Syndrome (Ichthyosis Alopecia Eclabion Ectropion Mental Retardation)

68. Birth Disorder Information Directory - M
Ankylosing Spondylarthritis. Marinesco Sjogren Like syndrome (JuvenileCataract with Cerebellar Atrophy, Myopathy and Mental Retardation)
http://www.bdid.com/defectm.htm

HOME
M
Machado Joseph Disease (Autosomic Dominant Spinocerebellar Ataxia, Autosomic Dominant Cerebellar Ataxia, Cerebelloolivary Atrophy, Olivopontocerebellar Atrophy, Pierre Marie Cerebellar Ataxia) Macrencephaly Macrocephaly Macrodactyly/Megalodactyly Macroglossia Macrogyria Macular Dystrophy

69. IComm: File Not Found!
March of Dimes Birth Defects Foundation http//modimes.org. marinescosjogrenSyndrome Support Website http//www.marinesco-sjogren.org.
http://www.icomm.ca/geneinfo/sg-m.htm
File Not Found
We're sorry, but the file you're looking for can't be found. You might want to try starting at our front page or a list of iComm accountholders , or you can search the site
This site was last updated on 30 August 2002.
iComm
Questions regarding the iComm web site should be sent to our webmaster

70. Mioti: Medical Condition
Marfan syndrome, • Marijuana Addiction. • Marinesco Sjogren syndrome,• Maroteaux Lamy syndrome. • Marshall Smith syndrome, • Marshall syndrome.
http://www.mioti.com/cat/condition/results.asp?Alpha=M

71. WebMD/Lycos - Article
Marden Walker syndrome Mareo Marfan syndrome Marfanoid Hypermobility syndrome MarieDisease MarieSainton Disease Marinesco Sjogren syndrome Marinesco-Garland
http://webmd.lycos.com/NR/internal.asp?GUID={CBDDF6E0-1ADA-4BE6-B791-DD4693ACC2E

72. Rare Musculoskeletal Disorders.
Coffin Lowry syndrome, Marfan syndrome, Sjogren syndrome. ConradiHunermann syndrome, Marinesco Sjogren syndrome, Split Hand Deformity.
http://www.orthoworld.com/support/rare-disorders.htm
OrthoWorld Home
Member Home
Rare Muscusloskeletal Disorders
Database
Achondrogenesis
Gordon Syndrome Proteus Syndrome ... Top

73. MSN Health -
Hypermobility syndrome Marie Disease Marie Strumpell Disease MarieSainton DiseaseMarie-Strumpell Spondylitis Marinesco Sjogren syndrome Marinesco-Garland
http://content.health.msn.com/NR/internal.asp?GUID={CBDDF6E0-1ADA-4BE6-B791-DD46

74. MSN Health -
Disease nord MarieStrumpell Spondylitis nord Marijuana Anonymous World Services- Drug Abuse shc Marinesco Sjogren syndrome nord Marinesco-Garland
http://content.health.msn.com/content/healthwise/67/16639.htm
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75. WebMD -
Marie Disease nord MarieSainton Disease nord Marijuana Anonymous World Services- Drug Abuse shc Marinesco Sjogren syndrome nord Marinesco-Garland
http://my.webmd.com/content/healthwise/67/16639.htm
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76. Progressive Cerebellar Syndromes
vasculitides, biotinidase deficiency, sphingomyelinase deficiency, neuroaxonaldystrophy, HallevordenSpatz, Marinesco Sjogren syndrome, Huntingtons disease
http://www.bme.jhu.edu/labs/chb/disorders/cerebell.html
Progressive cerebellar syndromes
The differential diagnosis of a progressive cerebellar syndrome includes vitamin E deficiency, lipoprotein disorders , neurocanthocytosis, Wilson disease MLD hexosaminidase deficiency , aminoacidurias including Hartnup disease , cerebrotendinous xanthomatosis, mitochondrial cytopathies, giant axonal neuropathy, hemochromatosis, adrenoleukodystrophy, Krabbe disease , Whipples disease, demyelinating disease, Behcets, progressive multifocal leukoencephalopathy, vasculitides, biotinidase deficiency, sphingomyelinase deficiency, neuroaxonal dystrophy, Hallevorden-Spatz, Marinesco Sjogren syndrome, Huntingtons disease, Creutzfeld-Jakob and GSS disease, inflammatory spinocerebellar degeneration, GAPN syndrome(antiMAG), thyroid disease, Chediak-Higashi , ataxia telangiectasia, superficial siderosis, heavy metal intoxications, drug (eg. Lithium and Dilantin) intoxication, nutritional, paraneoplastic and familial cerebellar degenerations (including Freidrichs, Joseph disease and other OPCAs including multiple system atrophy) and structural lesions including posterior fossa cysts, tumors, and vascular malformation; craniocervical junction anomalies, occasionally lesions in the frontal lobes or in the cervical spinal cord, and hydrocephalus.

77. NORD Rare Disease - Medical Transcription At Medword
Bipolar Mannosidosis Maple Syrup Urine Disease Marcus Gunn Phenomenon Marden Walkersyndrome Marfan syndrome Marinesco Sjogren syndrome Maroteaux Lamy syndrome
http://www.medword.com/rardisM.html
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Macroglossia

Macular Degeneration

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78. Istituto Giannina Gaslini - Cell Bank
MAPLE SYRUP URINE, 248600. MARFAN, 154700. marinescosjogren, 248800. MCCUNE-ALBRIGHTSYNDROME, 174800. MENKES, 309400. METACHROMATIC LEUCODYSTROPHY, 250100.
http://www.gaslini.org/DPPM/diaglist.htm
Gaslini Cell Line and DNA Bank
DIAGNOSIS LIST DIAGNOSIS OMIM Number
ACYL-CoA DEHYDROGENASE, LONG CHAIN, DEF. ADENOSINE DEAMINASE ADRENAL HYPERPLASIA III ADRENOLEUKODYSTROPHY ... ZELLWEGER Site by Dr. Mirella Filocamo Weekly update by Lucia Obino. Last update: 27/01/2003 10.17.58 Telethon grants have made this catalogue possible Best view 800x600 with Internet Explorer
Last update:27/01/2003 10.17.58

79. A Listing Of Disorders
Maple Syrup Urine Disease. Marden Walker syndrome. Marfan syndrome. Marinesco Sjogrensyndrome. Maroteaux Lamy syndrome. Marshall Smith syndrome. Marshall syndrome.
http://medschool.umaryland.edu/BTBank/Family/Disorders_M.htm
Brain and Tissue Bank
University of Maryland, Baltimore M Macular Degeneration Macular Degeneration, Polymorphic Madelung's Disease Maffucci Syndrome Malignant Hyperthermia Mannosidosis Maple Syrup Urine Disease Marden Walker Syndrome Marfan Syndrome Marinesco Sjogren Syndrome Maroteaux Lamy Syndrome Marshall Smith Syndrome Marshall Syndrome MASA Syndrome Mastocytosis Maxillofacial Dysostosis Maxillonasal Dysplasia, Binder Type May Hegglin Anomaly McArdle Disease McCune Albright Syndrome McKusick Type Metaphyseal Chondrodysplasia Meckel Syndrome Medium Chain Acyl CoA Dehydrogenase Deficiency Medullary Cystic Disease Medullary Sponge Kidney Megalocornea Mental Retardation Syndrome Meige Syndrome MELAS Syndrome Meleda Disease Melkersson Rosenthal Syndrome Melnick Needles Syndrome Meniere Disease Meningioma Menkes Disease MERRF Syndrome Mesenteritis, Retractile Metatropic Dysplasia I Microcephaly Microvillus Inclusion Disease Mikulicz Syndrome Miller Syndrome Mitral Valve Prolapse Syndrome Mixed Connective Tissue Disease (MCTD) Moebius Syndrome Monilethrix Morquio Syndrome Motor Neuron Disease Moyamoya Disease Mucha Habermann Disease Mucolipidosis IV Mucopolysaccharidosis Mulibrey Nanism Syndrome (Perheentupa Syndrome) Mullerian Aplasia Multiple Sclerosis Multiple Sulfatase Deficiency Mulvihill Smith Syndrome MURCS Association Muscular Dystrophy, Becker

80. Approach To A Case Of Ataxia
MSUD (Maple syrup urine disease); Marinesco – Sjogren syndrome (ataxia+ mental retardation + Bilateral cataracts + short stature);
http://www.pediatriconcall.com/fordoctor/DiseasesandCondition/approach_to_ataxia
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APPROACH TO A CASE OF ATAXIA UserName Password New Register
Dr Ira Shah
M.D, DCH(Gold Medalist), FCPS, DNB
Edited by
Dr Sarosh M Katrak MD, DM, FIAN
Consultant Neurologist
Ataxia is a disorder of movement characterized by The pathology causing ataxia can be anywhere in the cerebellum, or its connections with other parts of the nervous system. Differentiation between cerebellar and sensory ataxia: Sensory Ataxia: Cerebellar Ataxia:
  • Truncal Ataxia: The lesion is in the vermis of the cerebellum. The child has trouble keeping balance even while sitting and increases if asked to sit with legs crossed. This ataxia is better revealed on standing/running. The child has even more trouble keeping balance with eyes open. The gait is more lurching than seen in sensory ataxia (its almost staggering as seen in acute alcohol intoxication) and is more apparent when the patient is asked to turn quickly or hop on one foot. Titubation (to and fro bobbing of the head) may also be seen. The speech is usually slurred. Ataxia with disturbance predominant in one direction and dysmetria and hypotonia in unilateral limbs is seen in lesions in the ipsilateral cerebellar hemispheres. There is a tendency to veer off in the direction of the affected hemisphere.

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