The Canadian Society For Mucopolysaccharide Related Diseases Inc. Profile mannosidosis, Symptoms or effects with a line under them mean that Symptoms and Effects of mannosidosis. All items with information added will http://www.mpssociety.ca/display_diseases.php?uid=16
The Canadian Society For Mucopolysaccharide Related Diseases Inc. Testing for mannosidosis is not done during a standard pregnancy. If you already have a child with mannosidosis it is possible to have tests during a http://www.mpssociety.ca/display_details.php?uid=16&field=Diagnosis
Extractions: Vol. 41 No. 7, July 1984 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Halperin JJ Kolodny EH Contact me when this article is cited J. J. Halperin, D. M. Landis, L. A. Weinstein, I. T. Lott and E. H. Kolodny A 32-year-old man with mannosidosis had a gait disorder develop that was associated with communicating hydrocephalus. The gait disorder improved with ventriculoperitoneal shunting, but proximal muscle weakness remained. Biopsy specimens of muscle and nerve disclosed typical lysosomal inclusions in both tissues, as well as selective loss of unmyelinated axons.
Hill Health Topics A-Z - Alpha-Mannosidosis Alphamannosidosis. National Organization for Rare Disorders. Important It is possible that the main title of the report Alpha-mannosidosis is not the name http://www.healthwise.net/hillhealth/Content/StdDocument.aspx?DOCHWID=nord420&SE
SciQuest: Search Scientific Journals And Books Online Plasma alphamannosidase activity as a means of detecting mannosidosis Identification of mannosidosis heterozygotes - factors affecting normal plasma http://www.sciquest.org.nz/default.asp?pageid=2&nzvet_pgno=1&fulltext=&VSUBJECT1
Alpha Mannosidosis In Cattle Search for more data on alpha mannosidosis in cattle Click the Search button to search for more information on alpha mannosidosis in cattle within the http://www.cabicompendium.org/NamesLists/AHPC/Full/ALPHAA.htm
Extractions: The Compendium covers several hundred topics in food-animal production (cattle, buffaloes, sheep, goats, pigs, poultry), including distribution, husbandry, housing, handling, identification, transport, behaviour, nutrition, genetics, reproduction, techniques, welfare, slaughter, meat, milk, eggs, products, pictures, bibliography and legislation. Search for more data on alpha mannosidosis in cattle
Alpha-Mannosidosis Synonyms, Eastern Carolina Alphamannosidosis Synonyms - University Health Systems of Eastern Carolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county, http://www.uhseast.com/113457.cfm
Extractions: It is possible that the main title of the report Alpha-Mannosidosis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Alpha-mannosidosis is one of a group of very rare inherited disorders known as glycoprotein and related storage diseases. These disorders are caused by a defect in the breakdown of complex molecules in the cells, as a result of an enzyme deficiency. The enzyme that is lacking is known as alpha-D-mannosidase. The molecules that are not broken down are stored in the small components within cells known as lysosomes. The approximately 50 diseases in which this occurs are known as lysosomal storage diseases. In addition to alpha mannosidosis and a related disorder, beta mannosidosis, the lysosomal storage disorders include Fabry disease, Gaucher disease, cystinosis, aspartylglycosaminuria, the mucopolysaccharidoses, the mucolipidoses, and others.
Mannosidosis, Alpha, Eastern Carolina mannosidosis, Alpha University Health Systems of Eastern Carolina serves tarboro, ahoskie, edento, winsor, maxhead, dear county, outebanks counties in http://www.uhseast.com/117449.cfm
Extractions: Information about national and local self-help organizations and support groups. This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site. International network. Founded 1999. Provides emotional support for families affected by any oligosaccharide disorders of lysosomal storage. Offers educational resources for medical community. Promotes research to develop treatments. Phone support, literature, pen pals, information and referrals, newsletter, advocacy. Online message boards, chat rooms and e-mail discussions.
UNTSHC Clinic Digital Library mannosidosis Table of contents. Miscellaneous Beta mannosidosis Patient/Family Resources. Healthfinder (US DHHS) Homepage. Genetics List of documents http://unthsc-dl.slis.ua.edu/patientinfo/metabolism/inborn/lysosomalstorage/glyc
Guam Medical Libraries Digital Libraries Program mannosidosis, Alpha B Lyosomal Access document. Clinical Guidelines. National Guideline Clearinghouse MeSH browse Detailed search http://guam-dl.slis.ua.edu/clinical/metabolism/inborn/lysosomalstorage/glycoprot
Extractions: Clinical Resources by Topic: Metabolic Disorders Alpha Mannosidosis Clinical Resources Pediatrics Pathology Genetics Clinical Guidelines ... Miscellaneous Resources See also: MD Consult Reference Books: Table of contents Medical Library subscription INFO Otolaryngology and Facial Plastic Surgery (eMedicine): Table of contents Pediatrics Resources See also General Pediatrics Resources Behrman: Nelson Textbook of Pediatrics 17th Ed.-2004 (MD Consult):
Geneticalliance.org mannosidosis Support Groups. 2 organization(s) found. previous Page 1 of 1 next . Canadian Society for Mucopolysaccharide and Related Diseases Inc. http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t
Geneticalliance.org International Society for mannosidosis Related Diseases 3210 Batavia Avenue Baltimore, MD 21214 Phone 410.254.4903 Fax Website http//www.mannosidosis. http://www.geneticalliance.org/ws_display.asp?filter=support_groups_by_disease&t
Extractions: ISI Web of Science (4) Request Permissions PubMed PubMed Citation Articles by Roces, D. P. Articles by von Figura, K. Diego Prieto Roces Jianhe Peng Chiara Balducci Claes Andersson Ole Tollersrud Jens Fogh Aldo Orlacchio Tommaso Beccari Paul Saftig and Kurt von Figura Anatomisches Institut, University Kiel, Otto-Hahn-Platz 8, 24043 Kiel, Germany
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GEMdatabase - Selected Title TITLE, Alphamannosidosis. DESCRIPTION, This review focuses on the diagnosis, CONDITIONS, Lysosomal Disorders, mannosidosis, Metabolic Disorders http://www.gemdatabase.org/GEMDatabase/TitleDetailsOne.asp?TitleID=822
Beta-mannosidosis - Descipher Health External Links. Retrieved from http//www.descipher.com/health/info/Beta-mannosidosis . ViewsBetamannosidosis. From Descipher Health. http://www.descipher.com/health/info/Beta-mannosidosis
Extractions: ABSTRACT Alpha-mannosidosis is a rare, degenerative and chronic disease with multiple factors contributing to the degrees of progression. Since the patients are born healthy and exhibit a slow progression of clinical symptoms, an effective therapy initiated at early age could contribute to a normal evolution. This project is undertaken to reach such a therapy. Due to the complexity of the disease, the project requires an international effort with a plethoria of different techniques and disciplines involved. The aim is to reach a critical mass of understanding on both the molecular and pathophysiological level, and to use this knowledge to develop new strategies for therapy, using a mouse model of the disease. OBJECTIVES The main object of this project is to obtain a therapy for the lysosomal storage disease alpha-mannosidosis. To reach this goal the project will focus on the following objectives:
EUROPA - Research - Keyword Index All keywords Index feedback. The number of documents that contain the keyword alphamannosidosis is 1. Quality of Life - Cell factory - Community funded http://europa.eu.int/comm/research/index/pages_en__141.html
Rural Nurse Organization Clinic Digital Library mannosidosis, Beta A Lyosomal Access document. Clinical Guidelines. National Guideline Clearinghouse MeSH browse Detailed search http://ruralnurseorganization-dl.slis.ua.edu/clinical/metabolism/inborn/lysosoma
Extractions: Clinical Resources by Topic: Metabolic Disorders Beta Mannosidosis Clinical Resources Pediatrics Genetics Clinical Guidelines Clinical Trials ... Miscellaneous Resources See also: Pediatrics Resources See also General Pediatrics Resources Genetics Resources See also General Genetics Resources Clinical Guidelines Clinical Trials YAHOO - Health:Medicine:Clinical Trials
Extractions: Mannosidosis is a progressive storage disease caused by a deficiency of the enzyme alpha mannosidase in cats and is inherited by an autosomal recessive mode. The disease results in massive storage of sugars (oligosaccharides) in lysosomes of neuronal tissue and other cells Clinical signs occur in the first month of life and are progressive, leading to death by a few months. Although the deficiency can be determined by enzyme measurements in blood, there is a DNA test for one specific disease-mutation in several Persian and domestic shorthair/longhair cats. Clinical Signs: Beside failure to thrive and growth retardation, clinical signs include facial dysmorphia, ataxia, head and body tremors, skeletal deformities, behavioral changes, seizures and visual deficits. Cataracts and organomegaly may also be noted. Cytoplasmic vacuolization may be recognized in white blood cells. Affected Breeds:
