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Metachromatic Leukodystrophy: more detail

The Official Parent's Sourcebook on Metachromatic Leukodystrophy: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09-11
Leukodystrophies: Adrenoleukodystrophy, Canavan Disease, Pelizaeus-Merzbacher Disease, Metachromatic Leukodystrophy, Krabbe Disease
Metachromatic leukodystrophy: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Igor, MD, PhD Medica, 2005

lists with details

Metachromatic Leukodystrophy Of The Brain
metachromatic leukodystrophy of the Brain From the Virtual Pathology Museum, Department of Pathology, University of Connecticut Health Center.
http://radiology.uchc.edu/Code/1625.htm

Extractions: Metachromatic Leukodystrophy, Brain Metachromatic Leukodystrophy (low power) A low power view of white matter in MLD showing the collections of granular myelin debris and macrophages. MLD is most commanly seen in children who progress normally to a certain age than regress to coma and death. Adult forms are also seen. Image Contrib. by:Margaret Grunnet, M.D. UCHC Description by: Margaret Grunnet, M.D. ( 1724-5529) More Information
Metachromatic Leukodystrophy - General Practice Notebook
metachromatic leukodystrophy. metachromatic leukodystrophy is an autosomal recessive disorder of sphingolipid metabolism caused by
http://www.gpnotebook.co.uk/cache/-1818623963.htm

Extractions: metachromatic leukodystrophy Metachromatic leukodystrophy is an autosomal recessive disorder of sphingolipid metabolism caused by a deficiency of aryl-sulfatase A. The result is an accumulation of lipids such as galactosyl sulfatide. The disorder may be diagnosed prenatally by amniocentesis and assay of the aryl-sulfatase A activity.
MLD (metachromatic Leukodystrophy) - General Practice Notebook
MLD (metachromatic leukodystrophy). metachromatic leukodystrophy is an autosomal recessive disorder of sphingolipid metabolism caused
http://www.gpnotebook.co.uk/cache/1751842867.htm

Extractions: MLD (metachromatic leukodystrophy) Metachromatic leukodystrophy is an autosomal recessive disorder of sphingolipid metabolism caused by a deficiency of aryl-sulfatase A. The result is an accumulation of lipids such as galactosyl sulfatide. The disorder may be diagnosed prenatally by amniocentesis and assay of the aryl-sulfatase A activity.
Metachromatic Leukodystrophy - HUM-MOLGEN
Author, Topic metachromatic leukodystrophy. Natalia Olkhovich unregistered, posted 0317-2002 1252 PM Edit/Delete Message Reply w/Quote
http://www.hum-molgen.de/bb/Forum2/HTML/000101.html

Extractions: Administrative Options: Close Topic Archive/Move Delete Topic Hop to: Select a Forum or Archive List of Forums: Biotechnical requests and sources DIAGnostics - Clinical Research (professional requests) Ethical, legal and social implications Open Topic Forum List of Archives: Genetic News DIAGnostics - Clinical Research
Leukodystrophy,Refsum's Disease,Cerebrotendinous Xanthomatosis,Metachromatic Leu
Leukodystrophy,Refsum s Disease,Cerebrotendinous Xanthomatosis,metachromatic leukodystrophy,Globoid Leukodystrophy,Krabbe s Disease Included,Krabbe s
http://www.icomm.ca/geneinfo/leuk.htm

Extractions: Leukodystrophy,Refsum's Disease,Cerebrotendinous Xanthomatosis,Metachromatic Leukodystrophy,Globoid Leukodystrophy,Krabbe's Disease Included,Krabbe's Leukodystrophy,Adrenoleukodystrophy,Sudanophilic Leukodystrophy Included,Schilder's Disease,Pelizaeus-Merzbacher Brain Sclerosis,Alexanders Disease,Canavan's Disease Included,Canavan's Leukodystrophy Leukodystrophy is the name given to a group of very rare, progressive, metabolic, genetic diseases that affect the brain, spinal cord and often the peripheral nerves. Each of the leukodystrophies will affect one of the chemicals that make up the myelin sheath or white matter of the brain, causing the various types of leukodystrophy.
Metachromatic Leukodystrophy
Selected medical images OMIM metachromatic leukodystrophy. metachromatic leukodystrophy; metachromatic leukodystrophy; metachromatic leukodystrophy;
http://www.gfmer.ch/Genetic_diseases/Developmental_genetic_diseases/metachromati
Metachromatic Leukodystrophy
metachromatic leukodystrophy. from the Metachromic org). AN OVERVIEW OF MLD MLD stands for metachromatic leukodystrophy. Translated from
http://uscneurosurgery.com/glossary/m/metachromatic leukodystrophy.htm
Short Description Of Cell Lines. Pathology: Metachromatic Leukodystrophy, Late-i
Version 4.200205, Short description of cell lines. Pathology metachromatic leukodystrophy, lateinfantile *250100 OMIM record. - By
http://www.biotech.ist.unige.it/cldb/pat131.html
Short Description Of Cell Lines. Pathology: Metachromatic Leukodystrophy #249900
Version 4.200205, Short description of cell lines. Pathology metachromatic leukodystrophy 249900 OMIM record. By selecting the
http://www.biotech.ist.unige.it/cldb/pat214.html
Disease - Metachromatic Leukodystrophy - Hartford, Connecticut , Saint Francis C
Disease metachromatic leukodystrophy - courtesy of Saint Francis Care of Hartford, Connecticut, contemporary medicine with major clinical concentrations in
http://www.saintfranciscare.com/12889.cfm

Extractions: Back Back to main Health Information page Definition: Metachromatic leukodystrophy is an inherited disease characterized by the absence of the enzyme arylsulfatase A, which causes a material called cerebroside sulfate to accumulate in cells. This is toxic to the cell, especially neurons (the cells of the nervous system) and causes the problems of the disease. MLD is a member of a class of diseases called lysosomal storage disorders. In these diseases, patients lack a protein needed to metabolize the food we eat. Alternative Names: MLD; Arylsulfatase A deficiency Causes And Risk: Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait, which means that a person must inherit the defective gene from both parents to be affected. MLD has a wide range of symptoms. As with many other storage diseases, there are forms of early and delayed onset (late infant, juvenile, and adult types). The most common and most severe form is the late infant onset form, which has symptoms such as
Show-documents.asp
Health Tools Free Health Newsletter Health Info by Email What s New. The Cleveland Clinic, metachromatic leukodystrophy Written Information. Care Treatment.
http://www.clevelandclinic.org/health/search/do-query.asp?TopicId=1326
Metachromatic Leukodystrophy
metachromatic leukodystrophy. Definition metachromatic leukodystrophy is an inherited disease characterized by the absence of the
http://www.sjhsyr.org/sjhhc/hidc/ency/article/001205.htm

Extractions: Disease Injury Nutrition Poison ... Prevention Definition: Metachromatic leukodystrophy is an inherited disease characterized by the absence of the enzyme arylsulfatase A, which causes a material called cerebroside sulfate to accumulate in cells. This is toxic to the cell, especially neurons (the cells of the nervous system) and causes the problems of the disease. MLD is a member of a class of diseases called lysosomal storage disorders. In these diseases, patients lack a protein needed to metabolize the food we eat. Causes, incidence, and risk factors: Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait, which means that a person must inherit the defective gene from both parents to be affected. MLD has a wide range of symptoms. As with many other storage diseases, there are forms of early and delayed onset (late infant, juvenile, and adult types). The most common and most severe form is the late infant onset form, which has symptoms such as irritability decreased muscle tone muscle wasting , and the loss of the ability to walk in babies who have started walking. The disease progresses to
DISEASE: Metachromatic Leukodystrophy
DISEASE Featured Web Pages. metachromatic leukodystrophy $28.95 www.icongrouponline.com The Official Patient s Sourcebook on metachromatic leukodystrophy.
http://disease.bigtome.com/big/page/Metachromatic_Leukodystrophy
Blackwell Synergy - Cookie Absent
metachromatic leukodystrophy. Diffusion MR imaging and proton MR spectroscopy. RN Sener. A spectrum from the patient with metachromatic leukodystrophy (Fig.
http://www.blackwell-synergy.com/links/doi/10.1034/j.1600-0455.2003.00094.x/full

Extractions: Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.
Blackwell Synergy - Cookie Absent
metachromatic leukodystrophy. Diffusion MR imaging and proton MR spectroscopy. RN Sener. MRI appearances of metachromatic leukodystrophy. Pediatr. Radiol.
http://www.blackwell-synergy.com/links/doi/10.1034/j.1600-0455.2003.00094.x/enha

Extractions: Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.
OMIM - METACHROMATIC LEUKODYSTROPHY
http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250100
ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor
News about metachromatic leukodystrophy More news about metachromatic leukodystrophy . Books about metachromatic leukodystrophy
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/Neurologica

Extractions: Front Page Today's Digest Week in Review Email Updates ... Leukodystrophy Metachromatic Leukodystrophy (5 links) News about Metachromatic Leukodystrophy Brain Cell Transplants Potential Treatment For Multiple Sclerosis (November 1, 1999) full story (October 29, 1998) full story [ More news about Metachromatic Leukodystrophy Links about Metachromatic Leukodystrophy MLD Foundation - Support for Families With Metachromatic Leukodystrophy - Information, support, education and on-line networking for families throughout the world dealing with Metachromatic Leukodystrophy (MLD). NINDS - Metachromatic Leukodystrophy - A short information sheet compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
Biospace Glossary: Definitions
About the Glossary Basic Terms Term of the Day. metachromatic leukodystrophy. Sponsored by Society for In Vitro Biology (SIVB)
http://www.biospace.com/gls_detail.cfm?t_id=105615
Metachromatic Leukodystrophy, Late Infantile Form
metachromatic leukodystrophy, late infantile form. DESCRIPTION A form of leukoencephalopathy transmitted autosomal recessive. Characteristics
http://www.5mcc.com/Assets/SUMMARY/TP0585.html

Extractions: DESCRIPTION: A form of leukoencephalopathy transmitted autosomal recessive. Characteristics - accumulation of sphingolipid in neural and non-neural tissues with a diffuse loss of myelin in the central nervous system. The infantile form begins in the second year of life with blindness, motor disturbances, mental deterioration. Usual course - progressive.
Leukodystrophy
A little technical. metachromatic leukodystrophy (MLD) Infomration from the Duke University for Patients and their families. United Leukodystrophy Foundation.
http://www.ability.org.uk/Leukodystrophy.html

Extractions: Our Aims Services Stats ... Z Leukodystrophy Alexander disease mini information sheet - From the National Institutes of Health (USA) The Amn-Ald Community Pages - Support site for families dealing with the diseases Leukodystrophies). Canavan Foundation Canavan Research Fund - The Canavan Research Fund is a not-for-profit organization dedicated to pioneering research Cockayne Syndrome treatment, prevention and much more DrKoop.com - Adrenoleukodystrophy Leukodystrophy - CHORUS document on the different types of Leukodystrophy. A little technical. Metachromatic Leukodystrophy (MLD) - Infomration from the Duke University for Patients and their families. United Leukodystrophy Foundation Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments

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