WebMD Health - 404 Error Alpers progressive infantile poliodystrophy; Poliodystrophia Cerebri Progressiva;Progressive Cerebral Poliodystrophy; Diffuse Cerebral Degeneration in http://my.webmd.com/hw/raising_a_family/nord610.asp&e=747
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Encyclopedia: List Of Neurological Disorders Alpers disease, also called progressive infantile poliodystrophy, is a progressivedegenerative disease of the central nervous system that occurs in infants http://www.nationmaster.com/encyclopedia/List-of-neurological-disorders&e=747
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Alpers-disease&e=747: Web Search Results From Answers.com Alpers disease, also called progressive infantile poliodystrophy, is a progressivedegenerative disease of the central nervous system that occurs in http://www.answers.com/topic/alpers-disease&e=747
SRS Error ALPERS progressive infantile poliodystrophy ALPERS SYNDROME ALPERSHUTTENLOCHERSYNDROME NEURONAL DEGENERATION OF CHILDHOOD WITH LIVER DISEASE, PROGRESSIVE; http://srs.sanger.ac.uk/srsbin/cgi-bin/wgetz?%5Bomim-ID:203700%5D+-e&e=747
Mitochondrial Diseases Long name progressive infantile poliodystrophy. Symptoms seizures, dementia,spasticity, blindness, liver dysfunction, and cerebral degeneration. http://www.tsbvi.edu/Outreach/seehear/spring02/mitochondrial.htm&e=747
NORD - National Organization For Rare Disorders, Inc. Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis;Alpers progressive infantile poliodystrophy; Diffuse Cerebral Degeneration in http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Alpers%20Dise
Diffuse Degeneration Of Gray Matter With Cirrhosis - Talk Medical Alpers disease is also called progressive infantile poliodystrophy, and Alpersprogressive infantile poliodystrophy. Print this page http://www.talkmedical.com/medical-dictionary/4072/Diffuse-Degeneration-of-Gray-
Extractions: Tell a friend Diffuse degeneration of cerebral gray matter with hepatic cirrhosis, Alpers: A progressive disease of the nervous system characterized by spasticity (tightness), myoclonus and dementia and by liver problems with jaundice and cirrhosis. This disorder, first described by Alpers in 1931 as "Diffuse progressive degeneration of gray matter of cerebrum", usually begins early in life with convulsions. A continuous seizure (status epilepticus) is often the final event. Alpers diffuse degeneration of gray matter with hepatic cirrhosis is due to more than one cause. Some cases are inherited as autosomal recessive traits with both parents appearing normal but carrying one Alpers gene and each of their children, boys and girls alike, running a 1 in 4 risk of receiving both of the parental Alpers genes and suffering from this dread disease. Other cases of Alpers disease are due to disorders of oxidative phosphorylation, including mitochondrial DNA depletion syndromes. (Phosphorylation is the addition of phosphate to an organic compound, such as the addition of phosphate to ADP [adenosine diphosphate] to form ATP [adenosine triphosphate] or the addition of phosphate to glucose to produce glucose monophosphate, through the action of enzymes known as phosphotransferases or kinases.)
Extractions: 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. 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. 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.
Glossary Of Genetic Disorders. Alper Disease progressive infantile poliodystrophy. Cases of Alper disease maybe caused by disorders of oxidative phosphorylation, including mitochondrial http://aspin.asu.edu/geneinfo/glos-a.htm&e=747
Jan Geelen progressive infantile poliodystrophy (Alpers disease) with a defect in citricacid cycle activity in liver and fibroplasts. http://bss.ewi.utwente.nl/people/scientific/jan_geelen.doc/&e=747