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

The GAPS INDEX to Information on the Internet about Genetic Disorders and Birth Defects Genetic Information and Patient Services, Inc. (GAPS) HOME 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

Home List categories Eponyms A-Z Biographies by country ... Contact 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: 3-HYDROXYISOBUTYRIC ACIDURIA 3-METHYLGLUTACONIC ACIDURIA TYPE I 3-METHYLGLUTACONIC ACIDURIA, SEVERE OR TYPE III AAGENAES - RECURRENT CHOLESTASIS; LYMPHOEDEMA ... ZWETSLOOT (1989) - HOLOPROSENCEPHALY; MICROPHTHALMIA

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

document.write(''); var hwPrint=1; var hwDocHWID="nord610"; var hwDocTitle="Alpers Disease"; var hwRank="1"; var hwSectionHWID="nord610"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="NORD"; 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

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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

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map 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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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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