Geometry.Net - Health_Conditions: Alpers Disease

Rare Diseases List - Office Of Rare Diseases
Alopecia, epilepsy, pyorrhea, mental subnormality. alpers disease.Alpha 1antitrypsin deficiency. Alpha-2 deficient collagen disease.
http://ord.aspensys.com/diseases.asp

Extractions: An orphan or rare disease is generally considered to have a prevalence of less than 200,000 affected individuals in the USA. Certain diseases with more than 200,000 affected individuals are included but subpopulations of these conditions may be less than the prevalence standard for rare disease. This list includes rare diseases and conditions for which information requests have been made to the Office of Rare Diseases. It is updated on a regular basis. We welcome suggestions for additions to the list and your recommendations may be sent via email to: ord@od.nih.gov Please Note: The names of the conditions (listed in alphabetical order) may not necessarily be the most frequently used ones. Clicking on one of the names below will take you to a page that contains information specific for that disease. The links on that page will take you to several sources of information, including: ClinicalTrials.gov, an NIH site that lists ongoing clinical trials; Online Mendelian Inheritance in Man (OMIM), an NIH site authored and edited by Johns Hopkins University, with information on specific genetic diseases; and
Medicalseek - Search Engine For The Healthcare Industry
li= NORD alpers disease A brief description along with alternatename, followed by a list of resources for further information.
http://www.medicalseek.net/Conditions_and_Diseases_Neurological_Disorders_Neurod
Human And Animal Prion Diseases
GerstmannStraussler-Scheinker disease. Fatal familial insomnia. alpers disease?Animal prion diseases. Some prion diseases which occur in other species Scrapie.
http://www.mds.qmw.ac.uk/statgen/dcurtis/lectures/bsecjd1.html

Extractions: The following prion diseases are recognised in humans: Some prion diseases which occur in other species: Scrapie Bovine spongiform encephalopathy Transmissible mink encephalopathy Chronic wasting disease (mule deer, elk) Feline spongiform encephalopathy Zoological spongiform encephalopathy (eland, nyala, oryx, kudu, gemsbok, cheetah, puma, ocelot, ostrich)
Health Library
Allylamines for ringworm of the skin. Alopecia Areata. alpers disease. Alpha1-AntitrypsinDeficiency. Alpha-adrenergic agonists for urinary incontinence.
http://healthinfo.carolinas.org/library/healthguide/IllnessConditions/_SearchRes
A Listing Of Disorders
Albinism. Alexander's Disease. Alkaptonuria. Allan Herndon Syndrome. alpers disease.AlpersHuttenlocher Syndrome. Alpha-1-Antitrypsin Deficiency. Alport Syndrome.
http://medschool.umaryland.edu/BTBank/Family/Disorders_A.htm

Extractions: University of Maryland, Baltimore A Aarskog Syndrome Aase Syndrome Ablepharon Macrostomia Syndrome Acanthocheilonemiasis Acanthocytosis Acanthosis Nigricans Achard Thiers Syndrome Achondrogenesis Achondroplasia Acidemia, Isovaleric Acidemia, Methylmalonic Acidemia, Propionic Acrocallosal Syndrome, Schinzel Type Acrodermatitis Enteropathica Acrodysostosis Acromegaly Acromesomelic Dysplasia Acromicric Dysplasia ACTH Deficiency Acute Endocarditis Adams Oliver Syndrome Adie Syndrome Adrenal Hyperplasia, Congenital (General) Adrenoleukodystrophy Adrenomyeloneuropathy Afibrinogenemia, Congenital Agammaglobulinemias, Primary Agenesis of Corpus Callosum Agnosia, Primary Visual Agranulocytosis, Acquired Ahumada Del Castillo Syndrome Aicardi Syndrome Alagille Syndrome Albinism Alexander's Disease Alkaptonuria Allan Herndon Syndrome Alpers Disease Alpers-Huttenlocher Syndrome Alpha-1-Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia of Childhood Alveolitis, Extrinsic Allergic Alveolitis, Fibrosing Ameloblastoma Amelogenesis Imperfecta Amniotic Band Syndrome Amyloidosis Amyotrophic Lateral Sclerosis Andersen Disease Anemia, Aplastic
Metabolic Diseaese Children Self Help And Support Groups
Adrenal Hypoplasia Adrenomyeloneuropathy (AMN) Adrenoleukodystrophy (Leukodystrophy)Albrights Alcaptonuria Alexander (Leukodystrophy) alpers disease Alpha One
http://www.webhealth.co.uk/Self_Help_and_Support_Groups_R/Metabolic_Diseaese_Chi
A
Alopecia; alpers disease ( Cerebral Sclerosis, Diffuse); Alpha1 AntitrypsinDeficiency; Alport's Syndrome ( Nephritis, Hereditary);
http://www.fortunecity.co.uk/southbank/hornton/11/notes/topics.htm
Tusdata.com
Allergy ( Hypersensitivity); Alopecia; alpers disease ( DiffuseCerebral Sclerosis of Schilder); Alphavirus Infections; Alpha
http://www.tusdata.com/saglika/hast_a.htm

Extractions: Adli týpla ilgili bilmeniz gerekenler: Haklarýnýz ve Sorumluluklarýnýz B inlerce hastalýk hakkýnda ingilizce bilgi A B C D ... Albinism (Skin Diseases ..) Albinism, Ocular Alcoholism Alexanders Disease Alkalosis ... Arthritis, Rheumatoid (Musculoskeletal Diseases) Arthritis Arthrogryposis Arthropathy, Neurogenic Arthropod Diseases ... Z Yukarýdaki kaynaklara ek olarak ADAM Medical Encyclopedia ' dan 4,000 den fazla konuda açýklama istediðiniz her türlü bulgu, belirti ve testler hastalýðýn seyri hakkýnda bilgi.. yapýlacak, yapýlmasý gereken testler ve bu testlerin normal deðerleri.....(Not bu konularda bilgilenmek içindir. Kesinlikle doktora danýþmadan kendine taþhis koyup tedaviye baþlamayýnýz.) A B C D ... Z PARAMEDÝKAL Haber Kaynaklarý
Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : A Diseases Da
ALP low see Alkaline phosphatase levels low (plasma or serum) ALP raised see Alkalinephosphatase levels raised (plasma or serum) alpers disease Alpha 1
http://www.diseasesdatabase.com/sieve/disease_index_a.asp
Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : P Diseases Da
see Miliary aneurysms of retina Progressive familial intrahepatic cholestasis Progressiveinfantile poliodystrophy see alpers disease Progressive lipodystrophy
http://www.diseasesdatabase.com/sieve/disease_index_p.asp
Bernard Jacob Alpers (www.whonamedit.com)
Associated with alpers' disease. Associated eponyms alpers' disease A rare degenerativedisease of the brain, predominantly involving the grey matter.
http://www.whonamedit.com/doctor.cfm/185.html

Extractions: Bernard Jacob Alpers was educated at Harvard College and Harvard Medical School. a student of. After graduating in medicine from Harvard in 1923 he went to Europe for advanced training in neuropathology, working with Alfons Maria Jakob (1884-1931) in Hamburg. He subsequently began working in the Department of Neurosurgery at the University of Pennsylvania, and in 1939 became head of the Department of Nervous and Mental Disease at Jefferson Medical College, where he soon established an independent department of neurology. In his private time he enjoyed music and he had a life-long interest in religion.
NINDS Alpers' Disease Information Page
alpers' disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). What is alpers' disease? alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in
http://accessible.ninds.nih.gov/health_and_medical/disorders/alpersdisease_doc.h

Extractions: Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus Home About NINDS Disorders-you are in this section ... Find People The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury Studies with patients Research literature Press release NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us NINDS Alpers' Disease Information Page Alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in infants and children. It is an autosomal recessive disorder that is sometimes seen in siblings. First signs of the disease, which include intractable seizures and failure to meet meaningful developmental milestones, usually occur in infancy. Primary symptoms of the disease are developmental delay, progressive mental retardation, hypotonia (low muscle tone), spasticity (stiffness of the limbs), and dementia. Seizures may include epilepsia partialis continua, a type of seizure that consists of repeated myoclonic (muscle) jerks. Optic atrophy may also occur, often leading to blindness. And, although physical signs of chronic liver dysfunction may not be present, many patients suffer liver impairment leading to liver failure. While some researchers believe that Alpers' disease is caused by an underlying metabolic defect, no consistent defect has been identified.
NINDS - News And Events
Health. Sorry! There are no press releases for alpers' disease. Useyour browser's Back button to return to your previous activity.
http://www.ninds.nih.gov/health_and_medical/news.htm?url=/health_and_medical/dis
Biology - Past Issues Of Weekly Features
Symptoms, diagnosis, and treatment of alpers' disease. Information on research, community outreach and support.
http://genetics.about.com/science/genetics/library/blalp.htm
1Up Health > Alpers' Disease [Progressive Sclerosing Poliodystrophy] - Brain & N
What is alpers' disease? alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in
http://www.1uphealth.com/medical/disease/brain-neurological-disease/alpers%27-di
Health And Medical Information: Diseases And Conditions, Medical Dictionary, Pro
An alpers' disease article with some general information.
http://www.medicinenet.com/Script/Main/Art.asp?li=MNI&d=152&ArticleKey=8
Alpers' Disease (www.whonamedit.com)
alpers' disease A rare degenerative disease of the brain, predominantlyinvolving the grey matter. Also known alpers' disease Also known
http://www.whonamedit.com/synd.cfm/1459.html

Extractions: 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.
Rd.com:
General information about alpers' disease including the alternate names.
http://www.rd.com/common/nav/index.jhtml?articleId=8612597
Alpers Disease Factsheet
alpers disease. Download Factsheet. Not available. Feedback. Why is it calledalpers disease? The condition was first described in 1931 by Dr alpers.
http://www.ich.ucl.ac.uk/factsheets/illnesses/alpers_disease/
Directory Of Factsheets - Illnesses And Disease
Title, Created by Abdominal Wall Defects, NICU. alpers disease, CNS Neurology.Anaemia (Erythropoietin), Dialysis Unit. Anaemias (Rare anaemias), Host Defence.
http://www.ich.ucl.ac.uk/factsheets/illnesses/

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