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         Progressive Infantile Poliodystrophy:     more detail

1. ALPERS' PROGRESSIVE INFANTILE POLIODYSTROPHY
Features Listed For ALPERS' progressive infantile poliodystrophy. McKusick 203700. Abnormal liver (including function) Ataxia. Broad/barrel thorax. Camptodactyly. Camptodactyly/hammer toes. Cerebral
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?63

2. Alpers Disease,Progressive Infantile Poliodystrophy,Barth Syndrome,Cardiomyopath
Alpers Disease,progressive infantile poliodystrophy,Barth syndrome,CardiomyopathyNeutropeniaSyndrome/Lethal Infantile Cardiomyopathy,LIC,Beta-oxidation
http://www.icomm.ca/geneinfo/mitoch.htm
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DISORDERS GLOSSARY Mitochondrial Disorders
Alpers Disease (Progressive Infantile Poliodystrophy)
Barth syndrome (Cardiomyopathy-Neutropenia Syndrome) / Lethal Infantile
Cardiomyopathy (LIC)
Beta-oxidation Defects
Carnitine Deficiency and Disorders
Chronic Progressive External Ophthalmoplegia Syndrome (CPEO)
Kearns-Sayre Syndrome (KSS) Lactic Acidosis; Leber Hereditary Optic Neuropathy (LHON) Leigh's Disease (Subacute Necrotizing Encephalomyelopathy) Long-Chain Acyl-CoA Dehydrogenase (LCAD) Deficiency Luft Disease Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency Mitochondrial Cytopathy Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes (MELAS) Mitochondrial Encephalopathy Mitochondrial Myopathy Multiple Acyl-CoA Dehydrogenase (MAD) Deficiency / Glutaric Aciduria Type II Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF) Myoneurogastointestinal Disorder and Encephalopathy (MNGIE) Neuropathy Ataxia and Retinitis Pigmentosa (NARP) Pearson Syndrome; Pyruvate Carboxylase Deficiency

3. Alpers' Disease (www.whonamedit.com)
progressiva infantilis, progressive cerebral degeneration in infancy, progressive cerebral poliodystrophy, progressive infantile poliodystrophy, progressive poliodystrophy
http://www.whonamedit.com/synd.cfm/1459.html

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Whonamedit.com does not give medical advice.
This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor.
Alpers' disease Also known as:
Christensen's disease
Christensen-Krabbe disease Synonyms: Diffuse cortical sclerosis, familial degeneration of the cerebral grey matter in childhood, poliodysplasia cerebri, poliodystrophia cerebri progressiva, poliodystrophia progressiva corticalis, poliodystrophia cerebri progressiva infantilis, progressive cerebral degeneration in infancy, progressive cerebral poliodystrophy, progressive infantile poliodystrophy, progressive poliodystrophy. Associated persons: Bernard Jacob Alpers Erna Christensen Knud Haraldsen Krabbe Description: A rare degenerative disease of the brain, predominantly involving the grey matter. It is characterised by acute onset of severe convulsions leading to rapid intellectual and bodily breakdown. Other characteristics are blindness and deafness, myoclonus, spasticity, choroathetosis, cerebellar ataxia, growth retardation, and terminal decortication. Manifests in early childhood and usually causes death within months. In its familial form, the disorder is transmitted as an autosomal recessive trait.

4. Progressive Infantile Poliodystrophy - Medical Dictionary Definitions Of Popular
MedicineNet Home MedTerms medical dictionary AZ List progressive infantile poliodystrophy. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=8932

5. Alpers Disease - Medical Dictionary Definitions Of Popular Medical Terms
Alpers disease is also called Alpers progressive infantile poliodystrophy, progressiveinfantile poliodystrophy, diffuse degeneration of cerebral gray matter
http://www.medterms.com/script/main/art.asp?articlekey=8929

6. United Mitochondrial Disease Foundation - Medical Article List By Subject
The UMDF Medical Article List. Subject Alpers Disease (progressive infantile poliodystrophy) Back to the Subject List. United Mitochondrial Disease Foundation. We welcome any suggested additions to
http://www.umdf.org/data/query/alpers.htm
The UMDF Medical Article List
Subject: Alpers Disease (Progressive Infantile Poliodystrophy)
Back to the Subject List United Mitochondrial Disease Foundation We welcome any suggested additions to our list. Last updated: 26-Jun-98 REFERENCE FORMAT: Author Lastname; Firstname; Article Number; Article Title; Journal or Book; Year; Volume; Page Numbers Frydman ; M ; 1997* ; Alpers progressive infantile neuronal poliodystrophy: an acute neonatal form with findings of the fetal akinesia syndrome. ; American Journal of Medical Genetics ; 1993 ; 47(1) ; 31-6 Montine ; TJ ; 3814 ; Alpers' syndrome presenting with seizures and multiple stroke-like episodes in a 17-year-old male. ; Clin Neuropathol ; 1995 ; 14(6) ; 322-326 Narkewicz ; MR ; 2004 ; Liver involvement in Alpers disease. ; Journal of Pediatrics ; 1991 ; 119(2) ; 260-7 Wilson ; DC ; 1998* ; Progressive neuronal degeneration of childhood (Alpers syndrome) with hepatic cirrhosis. ; European Journal of Pediatrics ; 1993 ; 152(3) ; 260-2 Worle ; H ; 6380 ; Progressive cerebral degeneration of childhood with liver disease (Alpers Huttenlocher disease) with cytochrome oxidase deficiency presenting with epilepsia partialis continua as the first clinical manifestation. ; Clin Neuropathol ; 1998 ; 17(2) ; 63-8

7. Search: - Info.co.uk
Results for Progressive from Info.co.uk metasearch. Find better search results from the Web, Yellow Pages and White Pages quickly and easily! ALPERS' progressive infantile poliodystrophy. Features Listed For ALPERS' progressive infantile poliodystrophy. McKusick 203700
http://dpxml.infospace.com/infocom.uk/results?otmpl=dog/webresults.htm&qkw=P

8. Dysmorphic Syndromes
MENTAL RETARDATION; ALPERS progressive infantile poliodystrophy; ALPHATHALASSAEMIAMENTAL RETARDATION (16P DELETION); ALPHA THALASSAEMIA
http://www.hgmp.mrc.ac.uk/DHMHD/view_human.old
View Dysmorphic Syndrome Features
Select a dysmorphic syndrome by clicking on the relevant item:

9. Alpers Disease
Hepatic Cirrhosis. Alpers progressive infantile poliodystrophy. Poliodystrophia Cerebri Progressiva et al. Alpers progressive infantile neuronal poliodystrophy an acute neonatal
http://www.bchealthguide.org/kbase/nord/nord610.htm
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National Organization for Rare Disorders, Inc.
Alpers Disease
Important
It is possible that the main title of the report 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
  • Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis Alpers Progressive Infantile Poliodystrophy Poliodystrophia Cerebri Progressiva Progressive Cerebral Poliodystrophy Diffuse Cerebral Degeneration in Infancy
Disorder Subdivisions
  • None
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
  • Myoclonic Epilepsy Leigh's Disease Wernicke Encephalopathy Batten Disease Tay-Sachs Disease
General Discussion
Alpers Disease is a progressive neurologic disorder that begins during childhood. Symptoms include increased muscle tone with exaggerated reflexes (spasticity), seizures, loss of cognitive ability (dementia) and, in many cases, liver disease.

10. Alpers Disease,Alpers Diffuse Degeneration Of Cerebral Gray Matter With Hepatic
Alpers Disease,Alpers Diffuse Degeneration of Cerebral Gray Matter with HepaticCirrhosis,Alpers progressive infantile poliodystrophy,Poliodystrophia Cerebri
http://www.icomm.ca/geneinfo/alpers.htm
Alpers Disease,Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis,Alpers Progressive Infantile Poliodystrophy,Poliodystrophia Cerebri Progressiva,Progressive Cerebral Poliodystrophy,Diffuse Cerebral Degeneration in Infancy,Alpers Disease,Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis,Alpers Progressive Infantile Poliodystrophy,Poliodystrophia Cerebri Progressiva,Progressive Cerebral Poliodystrophy,Diffuse Cerebral Degeneration in Infancy
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

Genetic Information and Patient Services, Inc. (GAPS)
HOME
DISORDERS GLOSSARY Alpers Disease
also known as:
Alpers Diffuse Degeneration of Cerebral Gray Matter
with Hepatic Cirrhosis
Alpers Progressive Infantile Poliodystrophy
Poliodystrophia Cerebri Progressiva
Progressive Cerebral Poliodystrophy Diffuse Cerebral Degeneration in Infancy (as defined by the National Organization for Rare Disorders
Alpers Disease is a progressive neurologic disorder that begins during childhood.

11. P
progressive infantile poliodystrophy. Progressive Pallid Degeneration Syndrome Progressive Aphasia. Progeria. progressive infantile poliodystrophy. Progressive Pallid Degeneration
http://www.slider.com/Health/Conditions_and_Diseases/P.htm
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    12. Disease Directory : Alpers Disease,Progressive Infantile Poliodystrophy,Barth Sy
    Diseases Neurological Disorders Neurodegenerative Diseases Alpers Alpers Disease,progressive infantile poliodystrophy,Barth syndrome
    http://www.diseasedirectory.net/detailed/18092.aspx
    Wednesday, June 02, 2004 Neurological Disorders Neurodegenerative Diseases
    Alpers'

    Cockayne Syndrome
    ... Alpers' : Alpers Disease,Progressive Infantile Poliodystrophy,Barth syndrome ...
    Directory Listing
    Title: Alpers Disease,Progressive Infantile Poliodystrophy,Barth syndrome ...
    Description: Alpers Disease,Progressive Infantile Poliodystrophy,Barth syndrome,Cardiomyopathy-Neutropenia Syndrome/Lethal Infantile Cardiomyopathy,LIC,Beta-oxidation
    Date Added: 2/10/2004 12:21:28 PM
    URL: http://www.icomm.ca/geneinfo/mitoch.htm

    13. NORD - National Organization For Rare Disorders, Inc.
    Hepatic Cirrhosis. Alpers progressive infantile poliodystrophy. Diffuse Cerebral Degeneration Poliodystrophia Cerebri Progressiva. Progressive Cerebral Poliodystrophy. Disorder
    http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Alpers Diseas

    14. Untitled
    Developmental milestones are not being metà static vs. progressive process? Alpers Disease progressive infantile poliodystrophy. Menkes Syndrome trichopoliodystrophy
    http://www.ccn.upenn.edu/~aguirre/review_doc/Poduri_Gene2.doc
    ÐÏࡱá>þÿ PRþÿÿÿOÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿÿì¥ÁM ð¿î3bjbjâ=â= "P€W€W†+ÿÿÿÿÿÿl¦llll€ <A@òÿ¡

    15. OMIM - %203700 ALPERS DIFFUSE DEGENERATION OF CEREBRAL GRAY MATTER WITH HEPATIC
    ALPERS progressive infantile poliodystrophy ALPERS SYNDROME ALPERSHUTTENLOCHERSYNDROME NEURONAL DEGENERATION OF CHILDHOOD WITH LIVER DISEASE, PROGRESSIVE
    http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=203700

    16. Alpers Disease
    Cirrhosis; Alpers progressive infantile poliodystrophy; PoliodystrophiaCerebri Progressiva; Progressive Cerebral Poliodystrophy; Diffuse
    http://my.webmd.com/hw/raising_a_family/nord610.asp
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    Health Topics Symptoms ... For a Complete Report Alpers Disease Important It is possible that the main title of the report Alpers Disease 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
    • Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis Alpers Progressive Infantile Poliodystrophy Poliodystrophia Cerebri Progressiva Progressive Cerebral Poliodystrophy Diffuse Cerebral Degeneration in Infancy
    Disorder Subdivisions
    • None
    General Discussion Alpers Disease is a progressive neurologic disorder that begins during childhood. Symptoms include increased muscle tone with exaggerated reflexes (spasticity), seizures, loss of cognitive ability (dementia) and, in many cases, liver disease. Resources National Association for Visually Handicapped 22 West 21st Street New York, NY 10010

    17. Index
    Oto Syndrome Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic CirrhosisAlpers Disease Alpers progressive infantile poliodystrophy Alpha High
    http://my.webmd.com/hw/index/index-topics-A.asp
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    You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... Support Organizations Search the Help Health Topics Click a letter to see a list of topics beginning with that letter A B C D ... AZ A A Beta-2-Microglobulin Amyloidosis back to top A1AT Deficiency back to top AA Aarskog Syndrome Aarskog-Scott Syndrome AAS Aase Syndrome ... back to top AB Abdominal Migraine Abdominal Muscle Deficiency Syndrome Abdominal Wall Defect Abercrombie Syndrome ... back to top AC ACADL ACADM Deficiency Acampomelic campomelic "Dysplasia" Acanthocheilonemiasis ... back to top AD Adamantiades-Behcet's Syndrome Adamantinoma Adams Oliver Syndrome Adapting to reduced vision from age-related macular degeneration ... back to top AE AE AEC Syndrome back to top AF AF AFD Afibrinogenemia, Congenital

    18. Alpers Disease
    Synonyms. Alpers Diffuse Degeneration of Cerebral Gray Matter withHepatic Cirrhosis; Alpers progressive infantile poliodystrophy;
    http://www.meritcare.com/hwdb/showTopic.asp?pd_hwid=nord610

    19. Mitochondrial Conditions
    Alpers Disease (progressive infantile poliodystrophy); Barth syndrome (CardiomyopathyNeutropeniaSyndrome) / Lethal Infantile Cardiomyopathy (LIC); Beta
    http://www.kumc.edu/gec/support/mitochon.html
    Mitochondrial Conditions
    Alpers Disease (Progressive Infantile Poliodystrophy); Barth syndrome (Cardiomyopathy-Neutropenia Syndrome) / Lethal Infantile Cardiomyopathy (LIC); Beta-oxidation Defects; Carnitine Deficiency and Disorders; Chronic Progressive External Ophthalmoplegia Syndrome (CPEO); Kearns-Sayre Syndrome (KSS); Lactic Acidosis; Leber Hereditary Optic Neuropathy (LHON); Leigh Disease (Subacute Necrotizing Encephalomyelopathy); Long-Chain Acyl-CoA Dehydrogenase (LCAD) Deficiency; Luft Disease; Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency; Mitochondrial Cytopathy; Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes (MELAS); Mitochondrial Encephalopathy; Mitochondrial Myopathy; Multiple Acyl-CoA Dehydrogenase (MAD) Deficiency / Glutaric Aciduria Type II; Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); Myoneurogastointestinal Disorder and Encephalopathy (MNGIE); Neuropathy Ataxia and Retinitis Pigmentosa (NARP); Pearson Syndrome; Pyruvate Carboxylase Deficiency; Pyruvate Dehydrogenase Deficiency (PHD); Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency Respiratory Chain Disorders: Complex I: NADH dehydrogenase (NADH-CoQ reductase) deficiency, Complex II: Succinate dehydrogenase deficiency, Complex III: Ubiquinone-cytochrome c oxidoreductase deficiency, Complex IV: Cytochrome c oxidase (COX) deficiency, Complex V: ATP synthase deficiency

    20. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/P
    Ovarian Failure@ (6); Primary Progressive Aphasia@ (2); Progeria@(10); progressive infantile poliodystrophy@ (8); Progressive Pallid
    http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/P
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