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         Krabbe Disease:     more detail
  1. Krabbe's Disease: A Medical Dictionary, Bibliography, And Annotated Research Guide To Internet References by Icon Health Publications, 2004-10-08
  2. Krabbe disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Amie, MS Stanley, Rosalyn, MD Carson-DeWitt, 2005
  3. Krabbe Disease - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-18
  4. Krabbe disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amie, MS Stanley, 2005
  5. Leukodystrophies: Adrenoleukodystrophy, Canavan Disease, Pelizaeus-Merzbacher Disease, Metachromatic Leukodystrophy, Krabbe Disease
  6. Neurology, lectures for medical students and general practitioners by Knud H Krabbe, 1941
  7. Urolithiasis in dogs and cats by Agnete Krabbe, 1949

81. Healthsifter By Mary Pinkowish: Krabbe Disease Treated Successfully With Cord Bl
krabbe disease is one of several rare genetic disorders called lysosomal storage Listed below are links to weblogs that reference krabbe disease treated
http://marydpinkowish.typepad.com/healthsifter/2005/05/krabbe_disease_.html
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Healthsifter by mary pinkowish
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82. Globoid Cell Leukodystrophy (Krabbe Disease) - Diseases And Conditions - Blood A
Globoid Cell Leukodystrophy is a rare genetic disorder where the enzymegalactocerebrosidase is missing.
http://www.fairviewbmt.org/Diseases_and_Conditions/c_098530.asp
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BLOOD/MARROW TRANSPLANT HOME
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Fairview-University Blood and Marrow Transplant Services 500 Harvard St. Minneapolis, MN 55455 (Street Address) 420 Delaware St. SE MMC 803 Minneapolis, MN 55455 (Mailing Address) BMT Clinic Phillips-Wangensteen Building Clinic 5B, 5-100 516 Delaware St. SE Minneapolis, MN 55455
Globoid Cell Leukodystrophy (Krabbe Disease)
Globoid Cell Leukodystrophy (GLD) is a rare genetic disorder where the enzyme galactocerebrosidase (GALC) is missing. This results in a build up of globoid cells in the brain tissue.  Normally, nerve endings are covered with a myelin sheath which helps speed the communication of nerve impulses. The globoid cells cause the myelin to break down, affecting the patient’s development. As the disease progresses, the patient rapidly deteriorates. Because GLD is genetic, it is difficult to cure. Current approaches to GLD include genetic counseling for parents who are carriers of the disease, and improvements in early detection of the disease in unborn children.  For GLD patients, a variety of treatments have been tried. The goal of treatment is to get the missing GALC enzyme into the body. Unfortunately directly injecting it into the bloodstream has proven unsuccessful, since the enzyme cannot make it from there to the brain.  Injecting it directly into the brain has now worked either, because not enough of the enzyme is absorbed.

83. Democratic Underground - Jim Kelly's Son Hunter Dies Of Krabbe Disease At Age 8
Jim Kelly s son Hunter dies of krabbe disease at age 8 Kelly was given nomore than three years to live after being diagnosed with krabbe disease,
http://www.democraticunderground.com/discuss/duboard.php?az=view_all&address=215

84. WIVB TV4 Buffalo, NY - Our Apologies.
Hunter s Hope Finding a Cure for Krabbe s Disease they tell you, your childhas krabbe disease but , there s cord blood transplants right now
http://www.wivb.com/Global/story.asp?S=3689096

85. Drudge Retort: Jim Kelly's Son Dies Of Krabbe Disease
Jim Kelly s Son Dies of krabbe disease. Posted by rcade at 0507 PM permalink.AP Hunter Kelly, whose battle with a fatal nervous system disease
http://www.drudge.com/news/71538/jim-kellys-son-dies-krabbe-disease
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86. Demyelinating Diseases
krabbe disease (Globoid Cell Leukodystrophy) mini factsheets NINDS About Krabbe s Disease (Leukodystrophy, Globoid Cell/Krabbe s Disease) - (US)
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Diseases and Disorders Links pertaining to Demyelinating Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Adrenoleukodystrophy Alexander Disease Canavan Disease Demyelinating Diseases ... Neuromyelitis Optica
Demyelinating Diseases The Myelin Project [the Odone family et al.] - Washington DC (US) Brief Synopses of White Matter Disease: demyelinating , and White Matter Disease: dysmyelinating - CHORUS, Med College of Wisconsin (US)
Diffuse Cerebral Sclerosis of Schilder About Alpers disease - NINDS Alpers disease information - Institute of Child Health, NHS (UK)
Multiple Sclerosis About Multiple Sclerosis - Merck Manual, Home Edition Multiple Sclerosis: Current Status and Strategies for the Future - NAP 2001 (US) The US Nat'l Multiple Sclerosis Society including an extensive Source Book and a chapter about MS and Magnetic Resonance Imaging (MRI) Advances in Diagnosing Multiple Sclerosis - SW Med Center, Dallas, Sep 2003 (US)

87. Disease - Krabbe Disease - Detroit, Michigan
Disease krabbe disease - courtesy of Henry Ford Health System of Detroit, Michigan.
http://www.henryfordhealth.org/12220.cfm
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Disease - Krabbe disease
Definition: Krabbe disease is an inherited disorder characterized by a deficiency of the enzyme galactocerebroside beta-galactosidase (galactosylcereamidase). It results in destruction of myelin , a fatty material that surrounds and insulates many of the nerves. Alternative Names: Globoid cell leukodystrophy; Galactosylcerebrosidase deficiency; Galactosylcereamidase deficiency Causes And Risk: Krabbe disease is inherited as an autosomal recessive trait. It is most common among people of Scandinavian descent, but it generally affects about 1 in 150,000 infants. Absence of the enzyme galactocerebroside beta-galactosidase causes increasing destruction of myelin. This results in progressive destruction of the nervous system.
Krabbe disease has an early onset form and a late onset form. In the early form, symptoms begin in the first months of life with feeding problems and failure to thrive , unexplained fevers, and vomiting.

88. Newborn Screening News - NewbornScreening.Com
Hunter Kelly s valiant fight against Krabbe s Disease ends Not on the fieldor in his pursuit to find a cure for krabbe disease, the rare genetic
http://www.newbornscreening.com/
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August 26, 2005, 10:28 am
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Every year, about two million babies are born in the Philippines. Not many are aware, however, that 33,000 babies are at risk of life threatening disorders that could cause mental retardation and even death.
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August 19, 2005, 9:34 am Newborn screening: Early detection could help halt fatal genetic disease (Pepperell Free Press) wrote: PEPPERELL September is newborn screening awareness month, and folks like Barbara Forslind, whose three grandsons were born with Krabbe, an incurable genetic disease, want to add Krabbe to the roster of blood tests that newborns are routinely given.

89. Krabbe's Kids
If you would like your child s picture and/or story here please send us an email.Please take a look at these other site s dedicated to krabbe s disease.
http://www.krabbes.com/
This Page is dedicated to all of our children. Please follow the links below to learn about our terrific kids and learn what help is available. Trevor Leeker
Dalton Shell

Gina Rugari

Mikey Torres
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Anthoney Foster Joshua Cross ... Leandra Frye John D'Amico Kelly Blades Minna Larsson Eden Benson Sydney Trader(MLD) Aubrey Claflin Anthony Mattina Raegan Moore Souta Iwamae Linda Claverie Freddie Place ... Breanna Arthurs Taylor Todd Opp Britt Weijts Haley Sears Jhyrve Sears Anthony Shell ... Courtney Jo Rutherford Allie Julia Beatty Angela Maria Pitra Michelle Wright Rachell Jarrell Hunter Kelly Elijah Bonney Holli Startkweather Tanner Jurek-Plasky Megan Miles Liam Hammonds Melina Sevilla Makayla Lynn Pike Saschy Eichhorn Trevor Garbe Jason Forslind Logan Windley Ava Francisco Maddie Heflin Lucas Cole Nims Toi Imamure Olivia McCormick Degan Miles Dylan Kerdel Sandrine Dion Blake Ryan Harris Veronica Kreleger Jared Faria Krabbe Demographic Study sponsored by

90. Krabbe's Disease (www.whonamedit.com)
krabbe s disease An inborn neurodegenerative disorder of infancy due to theaccumulation of galactocerebroside in the tissues. Also known as krabbe s
http://www.whonamedit.com/synd.cfm/1457.html

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Krabbe's disease Also known as: Krabbe's syndrome I Krabbe's leukodystrophy Synonyms: Diffuse globoid body sclerosis, diffuse globoid cell cerebral scleroris, familial infantile diffuse brain sclerosis, galactocerebroside beta-galactosidase deficiency, galactosyl ceramide lipoidosis, galactosylceramide lipoidosis, globoid cell brain sclerosis, globoid cell cerebral sclerosis, globoid cell leukodystrophy, globoid cell sclerosis, globoid leukodystrophy, leukodystrophia cerebri. Associated persons: Knud Haraldsen Krabbe Description: An inborn neurodegenerative disorder of infancy due to the accumulation of galactocerebroside in the tissues. This is a result of a primary deficiency of galactocerebrosidase, the white matter of the brain, causing demyelination in the presence of inclusion bodies in the Schwann cells. The acute infantile form (90 percent of cases) is characterized by onset of symptoms before the age of 6 months and death by the end of first year of life, survival beyond 2 years being very rare. Clinically the child fails to thrive and develops seizures, deafness, blindness, cachexia, paralysis, and marked mental deficiency. The disease is assumed to be of genetical nature, but both dominant and recessive types have been described. There is also a rare juvenile and an adult form.

91. Globoid Cell Leukodystrophy (Krabbe S Disease) NeuroLearn
This is a unique feature of krabbe’s disease among the spingolipidoses. This differentiates krabbe’s disease from GM1 gangliosidosis which show normal
http://moon.ouhsc.edu/kfung/JTY1/NeuroHelp/ZNF5IE02.htm
Globoid Cell Leukodystrophy (Krabbe's Disease) NeuroLearn NeuroHelp Metabolic Lysosomal storage disorders, classification ... Gross Pathology BACKGROUND AND CLINICAL INFORMATION Head Summary: Globoid cell leukodystrophy (Krabbe’s disease, galactosylceramide lipidosis) is an autosomal recessive due to reduced lysosomal galactocerebroside b -galactosidase. The structural gene is on chromosome 14q24-q32. Both peripheral and central nervous systems are involved. Infantile onset is most common but later or adult onset cases have also been described. Clinically features vary with the age of onset. The infantile form is associated with death at 1-2 years of age. Pathologically , the brain is markedly atrophic and shows extensive demyelination associated with large, multinucleated cells (globoid cells). The white matter but not grey matter is predominantly affected. Crystalline needle-like inclusions that correspond to the globoid material are seen under electron microscope. Biochemistry:
  • Mutation of the galactocerebrosidase gene result in reduced enzymatic activity and decreased ability to degrade galactocerebroside that is found almost exclusively in myelin.

92. Health.iafrica.com | Doc Online | Ask The Doctor | Genetic Illness Krabbe's Dise
What is krabbe s disease? krabbe s disease is one of a rare, inheritablegroup of diseases known as lipidoses, which are disorders of lipid metabolism
http://health.iafrica.com/doconline/qa/genetic/krabbes_disease.htm
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93. Krabbe Disease Information Diseases Database
krabbe s disease,Galactosylceramidebeta-galactosidase deficiency,Globoid cellleucodystrophy, disease Database Information.
http://www.diseasesdatabase.com/ddb29468.htm
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Krabbe disease information
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3 synonyms or equivalents were found. Krabbe disease
aka/or
Galactosylceramide-beta-galactosidase deficiency
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Globoid cell leucodystrophy Krabbe disease: Definition(s) via UMLS Code translations and terms via UMLS Krabbe disease: specific web sites Send Krabbe disease to medical search engines (JavaScript enabled browsers only.) If your browser has no JavaScript you can still use these:
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Last major update 2005-09-03. The medical information here is presented for education, background reading and general interest. The Diseases Database is not a diagnostic or clinical decision-making tool. Please consult your own licensed physician regarding diagnosis and treatment of any medical condition! Content is not asserted complete or error free, please see also our

94. Krabbe's Disease (Globoid Cell Leukodystrophy) - OhioHealth
krabbe s disease is a rare, degenerative disorder of the nervous system, in whicha specific enzyme deficiency results in the destruction of myelin,
http://www.ohiohealth.com/healthreference/reference/2B1520EE-E635-426A-AC8865F6C

95. Leukodystrophy, Krabbe's
krabbe s Leukodystrophy is a rare inherited lipid storage disorder caused by This disease entry is based upon medical information available through the
http://my.webmd.com/hw/health_guide_atoz/nord379.asp
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Who We Are About WebMD Site Map You are in Medical Library Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Leukodystrophy, Krabbe's Important It is possible that the main title of the report Leukodystrophy, Krabbe's 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. Synonyms
  • Galactocerebrosidase (GALC) Deficiency Galactocerebroside Beta-Galactosidase Deficiency Galactosylceramide Lipidosis Galactosylceramidase Deficiency Krabbe's Disease Leukodystrophy, Globoid Cell Sphingolipidosis, Krabbe's Type Globoid Cell Leukoencephalopathy
Disorder Subdivisions
  • None
General Discussion Krabbe's Leukodystrophy is a rare inherited lipid storage disorder caused by a deficiency of the enzyme galactocerebrosidase (GALC), which is necessary for the breakdown (metabolism) of the sphingolipids galactosylceremide and psychosine. Failure to break down these sphingolipids results in degeneration of the myelin sheath surrounding nerves in the brain (demyelination). Characteristic globoid cells appear in affected areas of the brain. This metabolic disorder is characterized by progressive neurological dysfunction such as mental retardation, paralysis, blindness, deafness and paralysis of certain facial muscles (pseudobulbar palsy). Krabbe’s Leukodystrophy is inherited as an autosomal recessive trait.

96. Index.htm
krabbe s disease. Joseph s Story The Crabby krabbe s Mom s page allcontributions to this page are from moms. Men are welcome to look at this page,
http://home1.gte.net/robmil/
Joseph Miller Robinson September 12, 1996 - April 4, 1998 Krabbe's Disease Joseph's Story Joey has a baby sister! Click here to see her picture! Joseph's Memorial - pictures of Joseph's gravestone which was finally placed (7/15/99) Joseph's Journey - an overview of Joseph's life, including therapies we tried. Our Son Joseph - written by Joseph's Daddy. This was printed and placed in bulletins at Joseph's memorial services. Joseph's Photo Album - a few of our favorite memories. Physical, Speech and Aquatic Therapy - our experiences with Joseph. Positioning Devices - some things we came up with to help make Joseph more comfortable. When a Child Dies - a new page on the grieving process. Information will be added as we figure things out. And a little child will lead them prints and notecards to benefit Hunter's Hope. Friends - some beautiful children that we've met since learning the word Krabbe's.

97. Krabbe('s) Disease (Globoid Cell Leukodystrophy)
krabbe( s) disease (Globoid Cell Leukodystrophy, Galactosylceramidosis).krabbe s Family Network krabbes disease Homepage (CJ s page) krabbes disease
http://www.bdid.com/krabbe.htm

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98. GCL, Krabbe's Disease, Globoid Cell Leukodystrophy
aka krabbe s disease by George Jones. Globoid Cell Leukodystrophy is a degenerativedisease of the white matter of the brain and spinal cord, and also tied
http://www.barkbytes.com/medical/med0073.htm
Globoid Cell Leukodystrophy
GCL
a.k.a. Krabbe's Disease
by George Jones
Globoid Cell Leukodystrophy is a degenerative disease of the white matter of the brain and spinal cord, and also tied in with this is the loss of myelin , which is a fatty substance that forms the outer sheath around many nerve cells. What causes this loss is a genetic deficiency of an enzyme that is involved in breaking down certain lipids (fats) in the brain and spinal cord.
GCL has been seen in puppies as young as four weeks of age, and as late as five months. The disease progresses very rapidly, resulting in death usually within two to three months after the onset of the clinical signs of the disease. There is currently no treatment for GCL.
The clinical signs for GCL are: loss of coordination, failure to recognize familiar individuals (people or other pets), stumbling, blindness, weakness, tail tremors, total limb paralysis, and lack of response to pain. GCL has been found primarily in the bloodlines of West Highland White Terriers and Cairn Terriers, although it has been detected among other breeds as well. It is imperative that breeding stock be checked for this condition due to its being autosomal recessive (genetically passed on from one generation to another). In order for any autosomal recessive characteristic to appear in an offspring, both parents must either be carriers, or have the recessive characteristic. A blood test can determine the carrier (s) of this disease.

99. Jackson White
His son Hunter was diagnosed with krabbe s disease in 1997. Hunter s HopeFoundation s main focus in recent years is the issue of universal newborn
http://www.jacksonwhite.com/medical.htm
krabbe information On September 10th 2004, Jackson was diagnosed with Krabbe Leukodystrophy (pronounced "cra-BAY") or Krabbe's Disease. This is a rare, genetic disease that affects the myelin coating of the nervous system. Children with Krabbe are unable to produce an enzyme, GALC, which causes the myelin coating of their nerves to break down. Untreated, children with Krabbe Leukodystrophy progressively lose their motor skills, then their cognitive skills. They eventually enter a vegetative state and die within a few years after diagnosis. Jackson has a rare, slow-progressing form of Krabbe Disease. Because of this, he was found to be a candidate for a stem cell transplant to halt the progression of the disease. Jackson received his stem cell transplant at Duke University Medical Center, the top pediatric stem cell transplant center in the world. The source of his new cells was a unit of umbilical cord blood from a healthy baby. Stem cells get their name from their ability to develop into three types of blood cells: red blood cells, white blood cells and platelets. In a stem cell transplant, the stem cells from the cord blood grow inside bone marrow, creating a factory for new cells that will provide the critical enzyme that is lacking in Krabbe children. Though used like a bone marrow transplant as a source of stem cells, cord blood doesn't need to be as closely matched to the patient's tissue type, and it is available quickly, frozen and stored in blood banks. Cord blood units are collected from consenting mothers after delivery of their healthy, full-term baby and poses no risk to either mother or child. Donated umbilical cord blood is not tied up in the controversy surrounding stem cell research.

100. CareCure Forums - Umbilical Cord Blood Therapy Of Krabbe S Disease
Welcome to the CareCure Community. Our forums provide the latest information onspinal cord injury and related conditions.
http://sci.rutgers.edu/spinewire/forum/showthread.php?t=49880

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