CCHS Clinical Digital Library International Society for mannosidosis Related Diseases Homepage. Alpha mannosidosis Table of contents. Canadian MPS Society Homepage http://cchs-dl.slis.ua.edu/patientinfo/metabolism/inborn/lysosomalstorage/glycop
Extractions: Patient/Family Resources by Topic: Metabolic Disorders Alpha Mannosidosis Patient/Family Resources Miscellaneous See also: Canadian MPS Society: Homepage Miscellaneous Alpha Mannosidosis Patient/Family Resources MedlinePlus (National Library of Medicine) Health Topics: Index YAHOO - Health:Diseases and Conditions:Metabolic Diseases
Mannosidosis mannosidosis is a genetic disorder characterized by a lysosomal enzyme deficiency resulting in progressive mental and physical deterioration. A http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Alpha-mannosidosis: Information From Answers.com Alphamannosidosis a-mannosidosis is a genetic disorder that causes progressive mental and physical deterioration. http://www.answers.com/topic/alpha-mannosidosis
Extractions: showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Alpha-mannosidosis Wikipedia Alpha-mannosidosis is a genetic disorder that causes progressive mental and physical deterioration. A defective enzyme , which normally helps to break down complex sugars in the lysosome , causes sugar build up and impair cell function. This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see Mentioned In Alpha-mannosidosis is mentioned in the following topics: List of diseases starting with A Wikipedia information about Alpha-mannosidosis This article is licensed under the GNU Free Documentation License . It uses material from the Wikipedia article "Alpha-mannosidosis" More from Wikipedia Your Ad Here Jump to: Wikipedia Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Send this page Print this page Link to this page Tell me about: Home About Tell a Friend Buzz ... Site Map
Mannosidosis: Definition And Much More From Answers.com www.hgmp.mrc.ac.uk/dhmhdbin/hum-look-up?1051 Alpha-mannosidosis - Wikipedia, the free encyclopediaa-mannosidosis is a genetic disorder that causes progressive mental and physical Retrieved from http//en.wikipedia.org/wiki/Alpha-mannosidosis http://www.answers.com/topic/mannosidosis
Extractions: n. An inherited disorder caused by the deficiency of an enzyme necessary for the metabolism of mannose and characterized by mental retardation, kyphosis, and an enlarged tongue, with the accumulation of mannose in the body tissues. Mentioned In mannosidosis is mentioned in the following topics: Alpha-mannosidosis List of diseases starting with B List of diseases starting with A List of diseases starting with M ... List of biomedical topics, M Medical definition of mannosidosis Houghton Mifflin Company More from Medical Your Ad Here Jump to: Medical Mentioned In Or search: - The Web - Images - News - Blogs - Shopping Send this page Print this page Link to this page Tell me about: Home About Tell a Friend Buzz ... Site Map
Extractions: ORCID Home ORCID Cases Submit ORCID Case ORCID Presentation ... Contact ORCID Editor Dev. Team Editorial Board ISOST Global Consortium ... Orthogate Orthopaedic Rare Conditions Database (ORCID) Mannosidosis - Contents Cases Comments Bibliography Glycogen Storage Inherited disorder with skeletal and other effects. Best account on the Internet ? Cases Comments Bibliography Official ONIM names and synonyms 248500 MANNOSIDOSIS , ALPHA B, LYSOSOMAL Alternative titles; symbols ALPHA-MANNOSIDOSIS
Extractions: ORCID Home ORCID Cases Submit ORCID Case ORCID Presentation ... Contact ORCID Editor Dev. Team Editorial Board ISOST Global Consortium ... Orthogate Orthopaedic Rare Conditions Database (ORCID) Mannosidosis - Contents Cases Comments Bibliography Internet Links OMIM Mannosidosis A Online Mendelian Inheritance in Man database OMIM Mannosidosis B Support group with some clinical information NORD Mannosidosis Page (National Organization for Rare Disorders) Mannosidosis, the Web Site PubMed Citations with special reference to Orthopaedics Eckhoff DG, et al. [See Related Articles]
Alpha-Mannosidosis Alphamannosidosis is one of a group of very rare inherited disorders known as glycoprotein and related storage diseases. These disorders are caused by a http://www.bchealthguide.org/kbase/nord/nord420.htm
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.
Alpha-Mannosidosis - St. Joseph Mercy, Ann Arbor Michigan Alphamannosidosis - St. Joseph Mercy Health System Hospitals serving Ann Arbor, SE Michigan, Washtenaw County, Livingston County, Wayne County, http://www.sjmercyhealth.org/14473.cfm
NORD - National Organization For Rare Disorders, Inc. Alphamannosidosis is one of a group of very rare inherited disorders known as glycoprotein In addition to alpha mannosidosis and a related disorder, http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Alpha-Mannosi
GeneReviews: Alpha-Mannosidosis Your browser does not support HTML frames so you must view Alphamannosidosis in a slightly less readable form. Please follow this link to do so. http://www.geneclinics.org/profiles/a-mannosidosis
Mannosidosis Complete online version of The Encyclopaedia of Medical Imaging including text and images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/MANNOSIDOSIS.asp
Extractions: financial services our commitment our company Search Medcyclopaedia for: Search marked text (mark text before you click) Browse entry words starting with: A B C D ... amershamhealth.com Mannosidosis, deficiency of alpha mannosidase which leads to accumulation of glycoproteins in the tissues. Clinically, children have craniofacial dysmorphism, psychomotor retardation, cataracts and hearing loss. Radiologically, the features mimic those of mucopolysaccharidosis. There is brachycephaly, sometimes craniostenosis, widened ribs, flattened vertebrae with anterior beaking at the thoracolumbar junction, widening of the tubular bones with some irregularity of the metaphyses, a narrow basal segment to the iliac wings and osteoporosis.
SAS Centre : Assays : Genetic Enzymes : B-Mannosidosis b mannosidosis is a very rare disorder with only 10 cases in 7 families being known (Oct 1995). Clinical features vary widely but there has always been http://www.sas-centre.org/assays/genetic_enzymes/lysstodisbetamannosidosis.html
Extractions: b -mannosidosis is a very rare disorder with only 10 cases in 7 families being known (Oct 1995). Clinical features vary widely but there has always been mental retardation. There may be some dysmorphism, dysotosis multiplex and angiokeratoma (the latter seen only in two brothers). One case only was particularly severe.
SAS Centre : Assays : Genetic Enzymes : A-Mannosidosis Assays / Genetic Enzymes / amannosidosis. Broadly, the disease can be sub-divided into mild and severe types, both very rare, although there is probably a http://www.sas-centre.org/assays/genetic_enzymes/lysstodisamannosidosis.html
Extractions: Broadly, the disease can be sub-divided into mild and severe types, both very rare, although there is probably a continuum of phenotypes. In the most severe type there is hepatosplenomegaly, severe dysostosis multiplex, deafness, progressive mental retardation and often early death. In the milder form there is a later onset and more prolonged course with less severe dysostosis multiplex and mental retardation, but deafness is a major problem.
Mannosidosis Articles, Support Groups, And Resources mannosidosis articles, support groups, and resources for patients from Med Help International (www.medhelp.org) http://www.medhelp.org/HealthTopics/Mannosidosis.html
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Extractions: HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS This Article Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Embury, D. H. Articles by Jerrett, I. V. D. H. Embury and I. V. Jerrett Mannosidosis was diagnosed in four stillborn Galloway calves and an autolyzed full-term fetus from experimental matings of carrier animals. Gross lesions were moderate internal hydrocephalus, and pallor and enlargement of the liver and kidneys and arthrogryposis. Histologic changes in the central nervous system of each calf were marked foamy vacuolation of the cytoplasm of neurones in the cerebral cortex, thalamus and brainstem, and vacuolation of the Purkinje cells of the cerebellum. Spheroids were common throughout the brain and there was also consistent severe foamy cytoplasmic vacuolation of renal tubular epithelial cells and hepatocytes.
Extractions: HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS This Article Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Cited by other online articles PubMed PubMed Citation Articles by Alroy, J. Articles by Gavris, V. E. J. Alroy, U. Orgad, A. A. Ucci and V. E. Gavris Cells affected by locoweed (Astragalus lentiginosus) and Swainsona galegifolia toxicosis or mannosidosis exhibit similarities in their catabolism of N-linked glycoproteins and accumulation of cytoplasmic vacuoles. We used nine different biotinylated lectins as histochemical markers for specific sugars and avidin-biotin-peroxidase complex as a visualant to study the cells affected with these conditions. Since locoweed and Swainsona spp block mannosidase activity, we expected a similar lectin staining pattern in cells under these conditions as that seen in mannosidosis. Concanavalia ensiformis agglutinin, wheat germ agglutinin and
