Metachromatic Leukodystrophy metachromatic leukodystrophy. Causes and Risks metachromatic leukodystrophy(MLD) is transmitted as an autosomal recessive trait. http://www.rwjhamilton.org/Atoz/encyclopedia/article/001205.asp
Extractions: Medical Encyclopedia Encyclopedia Disease M -> Metachromatic leukodystrophy Metachromatic leukodystrophy Alternate Names: MLD; Arylsulfatase A deficiency Causes and Risks: Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait. 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 the most severe form) is the late infant onset form, which has symptoms such as irritability decreased muscle tone muscle wasting , the loss of the ability to walk. Debility is progressive with blindness seizures , and partial paralysis . Death occurs usually before age 10. Both the juvenile and adult forms have later onset but similar symptoms. In the adult and juvenile forms, psychosis and emotional disturbances are an important part of the illness. The juvenile form is fatal within a few years of diagnosis. The adult form may be drawn out over many years. Prevention: Genetic counseling is recommended for parents with a family history of metachromatic leukodystrophy.
Links To Other MLD-related Sites The Stennis Foundation is committed to raising public awareness regardingmetachromatic leukodystrophy (MLD). metachromatic leukodystrophy. http://www.stennisfoundation.org/vif/links.htm
Extractions: The Stennis Foundation is committed to raising public awareness regarding Metachromatic Leukodystrophy (MLD). One way this is done is through providing you, the reader, with information. This list is by no means exhaustive, nor is it intended for diagnostic purposes. Some of these sites do not pertain specifically to MLD. The views reflected in these websites are not necessarily those of The Stennis Foundation. Bethany's Hope Foundation The Myelin Project United Leukodystrophy Foundation Ashleys Angels ... stennisfoundation@stennisfoundation.org The Stennis Foundation: Raising public awareness regarding MLD, and raising funds for MLD research.
SmartEngine - SmartGuide ( DISEASE : Metachromatic Leukodystrophy ) DISEASE metachromatic leukodystrophy. A comprehensive manual for anyoneinterested in selfdirected research on metachromatic leukodystrophy. http://disease.smartengine.com/shell/smartpage/Metachromatic_Leukodystrophy
Leukodystrophy A little technical. metachromatic leukodystrophy (MLD) Infomration from the DukeUniversity 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
Type_Document_Title_here Back to Main List metachromatic leukodystrophy. metachromatic leukodystrophyis unusual among the leukodystrophies because, rather http://home.vicnet.net.au/~leuko/meta.html
Extractions: Back to Main List Metachromatic Leukodystrophy is unusual among the leukodystrophies because, rather than being caused by too little of a myelin sheath component, it is caused by too much of one. A lack of the enzyme arylsulfatase A leads to a build up of sulfatides, a component of the myelin sheath, in the patient's nervous system in various organs in the body such as the kidney, liver, and gall bladder. The sulfatides are not properly broken down when the enzyme is missing. Although Metachromatic Leukodystrophy, along with Adrenoleukodystrophy, is probably the most frequently observed leukodystrophy, the reason why this increase in sulfatide levels causes demyelination is as yet unknown MLD is an autosomal recessive type of disorder, and manifests in three types: Late Infantile, with onset of symptoms between six months and two years of age; Juvenile, with onset of symptoms after age four until age sixteen years; Adult, with onset of symptoms after age sixteen and characterized by psychiatric disturbances evolving to dementia. Only one form of MLD is seen within a family.
Metachromatic Leukodystrophy Clinical Resources Clinical Resources by Topic Metabolic Disorders. metachromatic leukodystrophyClinical Resources. metachromatic leukodystrophy List of documents. http://baptistnashville-dl.slis.ua.edu/clinical/metabolism/inborn/lysosomalstora
Extractions: Clinical Resources by Topic: Metabolic Disorders Metachromatic Leukodystrophy Clinical Resources Pediatrics Radiology Pathology Genetics ... Miscellaneous Resources See also: Neurology (eMedicine): Table of contents CliniWeb: Homepage (includes links to targeted PubMed MEDLINE searches) Pediatrics Resources See also General Pediatrics Resources Pediatric Database (PEDBASE) List of documents Radiology Resources See also General Radiology Resources Pathology Resources eAtlas of Pathology (Univ of Connecticut): Table of contents Diseases of Brain: List of documents Metachromatic Leukodystrophy (Low Power): Access document Metachromatic Leukodystrophy (Low Power):
Silver Hill Hospital Digital Library Clinical Resources by Topic Metabolic Disorders. metachromatic leukodystrophyClinical Resources. metachromatic leukodystrophy Access document. http://silverhillhospital-dl.slis.ua.edu/clinical/metabolism/inborn/lysosomalsto
Extractions: Clinical Resources by Topic: Metabolic Disorders Metachromatic Leukodystrophy Clinical Resources Pediatrics Radiology Pathology Genetics ... Miscellaneous Resources See also: CliniWeb: Homepage (includes links to targeted PubMed MEDLINE searches) Pediatrics Resources See also General Pediatrics Resources Pediatric Database (PEDBASE) List of documents Radiology Resources See also General Radiology Resources Pathology Resources Genetics Resources See also General Genetics Resources Online Mendelian Inheritance in Man: Homepage Metachromatic Leukodystrophy: Access document Metachromatic Leukodystrophy, Adult Onset:
Metachromatic Leukodystrophy The summary for this Korean page contains characters that cannot be correctly displayed in this language/character set. http://neurology.or.kr/familial cases-J/tsld015.htm
Metachromatic Leukodystrophy The summary for this Korean page contains characters that cannot be correctly displayed in this language/character set. http://neurology.or.kr/familial cases-J/sld015.htm
Metachromatic Leukodystropy metachromatic leukodystrophy. Adult Forms of metachromatic leukodystrophy Clinicaland Biochemical Approach. Developmental Neuroscience, 13; 211215 (1991). http://www.clevelandclinic.org/health/health-info/docs/1300/1304.asp?index=6067
Health Library Find Information On Metachromatic Leukodystrophy Find information on metachromatic leukodystrophy at MerckSource. Learn more Metachromaticleukodystrophy. Definition metachromatic leukodystrophy http://www.mercksource.com/pp/us/cns/cns_hl_adam.jspzQzpgzEzzSzppdocszSzuszSzcns
Guam Medical Libraries Digital Libraries Program metachromatic leukodystrophy Patient/Family Resources. metachromatic leukodystrophyAccess document. HealthSouth Disease Encyclopedia Table of contents http://guam-dl.slis.ua.edu/patientinfo/metabolism/inborn/lysosomalstorage/sphing
Extractions: Patient/Family Resources by Topic: Metabolic Disorders Metachromatic Leukodystrophy Patient/Family Resources Spanish Miscellaneous See also: United Leukodystrophy Foundation Access document MEDLINE plus Medical Encyclopedia: Table of contents Spanish Miscellaneous Metachromatic Leukodystrophy Patient/Family Resources Healthfinder (US DHHS): Homepage National Library of Medicine MEDLINE plus Health Topics: Index YAHOO - Health:Diseases and Conditions:Metabolic Diseases
Leukodystrophy Leukodystrophy CHORUS document on the different types of Leukodystrophy. MetachromaticLeukodystrophy (MLD) - The metachromatic leukodystrophy (MLD) Page. http://www.health-nexus.com/leukodystrophy.htm
Extractions: Health-Nexus.Net Health-Nexus.Org The #1 Health information site Search Health-Nexus for: Match ALL words Match ANY word Email this page to a friend ! Post a question or comment on our Message Board Home Page Health Specialties Health News ... Alternative Health Options Substance Abuse Animal Health Search: Books Magazines Video Keywords: Find it Here Leukodystrophy United Leukodystrophy Foundation - UNITED LEUKODYSTROPHY FOUNDATION 2304 Highland Drive * Sycamore, Illinois USA 60178 * Phone: (800) 728-5483 * FAX: (815) 895-2432 The United Leukodystrophy Foundation (ULF), incorporated in 1982, is a nonprofit, voluntary health organization. Leukodystrophy - CHORUS document on the different types of Leukodystrophy.
2718 Mutation Analysis Of Krabbe Disease And Metachromatic Program Nr 2718 Mutation analysis of Krabbe Disease and metachromatic leukodystrophyin Portugal. AML Marcao, OMO Amaral, EM Pinto, MC Sa Miranda. http://www.faseb.org/genetics/ashg99/f2718.htm
Extractions: Disease Reference Injury Reference Test Reference Nutrition Reference ... Symptoms Reference Disease Injury Nutrition Poison ... Z Definition: Metachromatic leukodystrophy is an inherited metabolic storage disease characterized by the absence of the enzyme arylsulfatase A and increased storage of sulfatide. Causes, incidence, and risk factors: Metachromatic leukodystrophy (MLD) is transmitted as an autosomal recessive trait. 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 the most severe form) is the late infant onset form, which has symptoms such as irritability decreased muscle tone muscle wasting , the loss of the ability to walk. Debility is progressive with blindness seizures , and partial paralysis . Death occurs usually before age 10.
ClinicalTrials.gov - Linking Patients To Medical Research Search Query Details. No studies were found for NINDS metachromatic leukodystrophy InformationPage ALLFIELDS. metachromatic leukodystrophy ALL-FIELDS, TryIt! http://www.clinicaltrials.gov/search/term=NINDS Metachromatic Leukodystrophy Inf
Middle Tennessee Medical Center Digital Library Clinical Resources by Topic Metabolic Disorders. metachromatic leukodystrophyClinical Resources. metachromatic leukodystrophy Access document. http://mtmc-dl.slis.ua.edu/clinical/metabolism/inborn/lysosomalstorage/sphingoli
Extractions: Clinical Resources by Topic: Metabolic Disorders Metachromatic Leukodystrophy Clinical Resources Pediatrics Radiology Pathology Genetics ... Miscellaneous Resources See also: CliniWeb: Homepage (includes links to targeted PubMed MEDLINE searches) Pediatrics Resources See also General Pediatrics Resources Pediatric Database (PEDBASE) List of documents Radiology Resources See also General Radiology Resources Pathology Resources Genetics Resources See also General Genetics Resources Online Mendelian Inheritance in Man: Homepage Metachromatic Leukodystrophy: Access document Metachromatic Leukodystrophy, Adult Onset: