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         Mannosidosis:     more detail
  1. Mannosidosis: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Linnea, MS Wahl, 2005

21. Short Description Of Cell Lines. Pathology Mannosidosis, Alpha B
Version 4.200205, Short description of cell lines. Pathology mannosidosis,alpha b, lysosomal *248500 OMIM record. By selecting
http://www.biotech.ist.unige.it/cldb/pat111.html

22. Health Library - Mannosidosis, Alpha
mannosidosis, Alpha. Self Help Clearinghouse. Int'l Society for mannosidosisand Related Diseases, Inc. International network.
http://bhagh.nhshealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29man

23. Health Library - Mannosidosis, Alpha
mannosidosis, Alpha. Self Help Clearinghouse. Int'l Society for mannosidosisand Related Diseases, Inc. International network.
http://yalenewhavenhealth.org/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29m

24. Health Library - Mannosidosis, Alpha
Saint Luke's Health System eLibrary. mannosidosis, Alpha. Self Help Clearinghouse.Int'l Society for mannosidosis and Related Diseases, Inc.
http://hvelink.saint-lukes.org/library/healthguide/SelfHelp/topic.asp?hwid=shc29

25. Health Library - Mannosidosis
mannosidosis. mannosidosis is a genetic disorder characterized by a lysosomal enzymedeficiency resulting in progressive mental and physical deterioration.
http://health_info.nmh.org/Library/HealthGuide/IllnessConditions/topic.asp?hwid=

26. Mannosidosis
only. mannosidosis,, Print this article, deficiency of alpha mannosidasewhich leads to accumulation of glycoproteins in the tissues.
http://www.amershamhealth.com/medcyclopaedia/Volume VII/MANNOSIDOSIS.asp
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*For Medical Professionals only, registration required 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.
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27. ORCID Mannosidosis Bibliography
mannosidosis Bibliography. Internet Links. OMIM mannosidosis A OnlineMendelian Inheritance in Man database. OMIM mannosidosis B.
http://www.orthogate.com/orcid/mannobib.htm
ORCID
Orthopaedic Rare Conditions Internet Database
Mannocidosis Contents
Cases Comment Bibliography ... ORCID Contents
Mannosidosis - 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]
Severe destructive polyarthropathy in association with a metabolic storage disease. A case report.
J Bone Joint Surg Am. 1992 Sep;74(8):1257-61.
Wall DA, et al. [See Related Articles]
Bone marrow transplantation for the treatment of alpha-mannosidosis.
J Pediatr. 1998 Aug;133(2):282-5.

28. ORCID Mannosidosis Case
mannosidosis Cases. I would like to know if anyone has experiencewith implanting a THP in a hip destructed by mannosidosis. This
http://www.orthogate.com/orcid/mannocase.htm
ORCID
Orthopaedic Rare Conditions Internet Database
Mannocidosis Contents
Cases Comment Bibliography ORCID Home Page ORCID Contents
Mannosidosis - Cases I would like to know if anyone has experience with implanting a THP in a
hip destructed by mannosidosis.
This is a rare disease, where, because of defective mannisidase, normal
degradation of glycoproteins is not possible. This causes (among others)
mental retardation, skeletal problems and joint destruction. This joint
destruction is said to be resembling rheumatoid arthritis.
Our reumatologist presented me a 19 year old girl with a destructed
right hip and severe pain. As you can see from the X-rays, it took some years to develop, and it looks to me that the pathology lies primarily in the bone of the acetabulum: The bone gradually disapears while the joint space in the beginning is not narrowed.(Not like RA) Since her life expectancy is limited and she is very disabled, a THP seems to be the only option. A large homologous bone graft (impaction grafting) will be nessesary, and I think there are two problems:

29. UNTSHC Clinic Digital Library
Beta mannosidosis Patient/Family Resources. Miscellaneous Beta mannosidosisPatient/Family Resources Healthfinder (US DHHS) Homepage
http://unthsc-dl.slis.ua.edu/patientinfo/metabolism/inborn/lysosomalstorage/glyc
Patient/Family Resources by Topic: Metabolic Disorders
Beta Mannosidosis Patient/Family Resources
Miscellaneous See also:

30. International Society For Mannosidosis And Related Diseases, Inc
Return to Search Page International Society for mannosidosis and Related Diseases,Inc. Website http//www.mannosidosis.org Email info@mannosidosis.org.
http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Inte

31. 1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders
Conditions and Diseases Genetic Disorders mannosidosis . Provides support, educationand research on Alpha mannosidosis and other similar disorders.
http://www.1uphealth.com/links/genetic-disorders-mannosidosis.html
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Sites Information about the organization, its mission and services. Provides support, education and research on Alpha Mannosidosis and other similar disorders. NORD - Mannosidosis Offers alternative names, a general discussion and resources. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites.

32. 1Up Health > Health Links Directory >Conditions And Diseases:Genetic Disorders:M
1UpHealth Health Directory Conditions_and_Diseases Genetic_Disordersmannosidosis mannosidosis is a genetic disorder characterized
http://www.1uphealth.com/links/desc-640.html
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... Mannosidosis Mannosidosis is a genetic disorder characterized by a lysosomal enzyme deficiency resulting in progressive mental and physical deterioration.
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33. Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Mannosidosis
Similar pages Roche Lexikon Medizin (4. Aufl.) Mannosidasemangel-Syndrom, - Translate this page Man nosi da se mangel-Syndrom, mannosidosis. engl. mannosidosis. autosomal-rezessiverbliche Störung des Glykoprotein-Abbaus infolge
http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Mannosidosis

34. Mannosidosis : Meddie Health Search
ITEMS LINKS International Society for mannosidosis Related DiseasesInformation about the organization, its mission and services.
http://www.meddie.com/search/Health/Conditions_and_Diseases/Genetic_Disorders/Ma
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35. WebGuest - Open Directory : Health : Conditions And Diseases : Genetic Disorders
Sites International Society for mannosidosis Related Diseases Information about the organization, its mission and services.
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the entire directory only in Genetic_Disorders/Mannosidosis Top Health Conditions and Diseases Genetic Disorders : Mannosidosis

See also:
Sites:
  • - Information about the organization, its mission and services. Provides support, education and research on Alpha Mannosidosis and other similar disorders.
  • NORD - Mannosidosis - Offers alternative names, a general discussion and resources.
Last update: 8:20 PT, Saturday, March 17, 2001
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36. LysosomalStorageDisordersAlpha-Mannosidosis
amannosidosis. Broadly, the disease can be sub-divided into mild and severe types,both very rare, although there is probably a continuum of phenotypes.
http://www.sas-centre.org/genetic/genpages/lysstodisamannosidosis.html
a -Mannosidosis 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. Enzyme Tests:
Deficiency of lysosomal a -mannosidase is the primary defect. Back to Lysosomal Storage Disorders Index

37. Alpha-Mannosidase
Uses and Limitations of the Method Deficiency of lysosomal ámannosidaseis the primary defect in a-mannosidosis, leading to storage of various
http://www.sas-centre.org/genetic/genpages/lysstodisamannosidase.html
a -Mannosidase Principle of Method:
Hydrolysis of the synthetic substrate 4-methylumbelliferyl- a -D-mannopyranoside at acid pH is followed by measuring the fluorescence of the liberated 4-methylumbelliferone after stopping the reaction with alkaline buffer. Uses and Limitations of the Method:
a
-mannosidosis , leading to storage of various oligosaccharides with an a- mannose residue at their non-reducing terminals. a -mannosidase is elevated in plasma from patients with I-cell disease and pseudo-Hurler polydystrophy , and is a useful enzyme to measure in amniotic fluid for prenatal diagnosis of these disorders. Prenatal diagnosis of a -mannosidosis is available by CVS or amniocentesis. Heterozygote detection may be possible in affected families but is not offered for screening in the general population. a -mannosidosis patients exhibit a distinctive abnormal oligosacchariduria, and this is a good screening test before definitive assay of the enzyme. Assay of a -mannosidase is included in all our lysosomal enzyme screening procedures.
Specimen Requirements:
Blood.

38. Health Library - Mannosidosis
mannosidosis. mannosidosis is a genetic disorder characterized by a lysosomal enzymedeficiency resulting in progressive mental and physical deterioration.
http://www.laurushealth.com/library/healthguide/illnessconditions/topic.asp?hwid

39. Searchalot Directory For Mannosidosis
Related Web Sites. International Society for mannosidosis Related Diseases Information about the organization, its mission and services.
http://www.searchalot.com/Top/Health/ConditionsandDiseases/GeneticDisorders/Mann
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  • - Information about the organization, its mission and services. Provides support, education and research on Alpha Mannosidosis and other similar disorders.
  • NORD - Mannosidosis - Offers alternative names, a general discussion and resources.
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40. Health Library - Mannosidosis, Alpha
mannosidosis, Alpha. Self Help Clearinghouse. International Society for mannosidosisand Related Diseases, Inc. International network.
http://www.billingsclinic.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29m

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