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Abetalipoproteinemia:     more detail

Abetalipoproteinemia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Scott, MS, CGC Polzin, 2005 Abetalipoproteinemia Abetalipoproteinemia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19 Bassen-Kornzweig syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005

lists with details

1. Abetalipoproteinemia
   abetalipoproteinemia. rare, autosomal recessive; malabsorption offat. progressive neurologic deterioration; retinitis pigmentosa. In  
   http://chorus.rad.mcw.edu/doc/00432.html

2. ABETALIPOPROTEINEMIA
   Advertisement. abetalipoproteinemia A rare congenital disorder that causes the body to not produce chylomicrons, low  
   http://www.medhelp.org/glossary/new/GLS_0033.HTM
   
   Extractions: ABETALIPOPROTEINEMIA - A rare congenital disorder that causes the body to not produce chylomicrons, low density lipoprotein LDL ), and very low density lipoprotein VLDL ). Individuals with this condition are unable to properly digest fats. Other findings include ataxia peripheral neuropathy , and other forms of nerve dysfunction. Treatment includes vitamin E

3. Abetalipoproteinemia
   Article describes abetalipoproteinemia, its diagnosis, and treatment. abetalipoproteinemia (also known as BassenKornzweig syndrome) is an inherited disorder that problems caused by lack of  
   http://rarediseases.about.com/library/weekly/aa072601a.htm
   
   Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Email to a friend Print this page Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. Suggested Reading Internet links on abetalipoproteinemia Elsewhere on the Web Abetalipoproteinemia discussion group Most Popular The Elephant Man's Bones Reveal Mystery ALD and Lorenzo's Oil Prune Belly (Eagle-Barrett) Syndrome Progeria Syndromes ... Mad Cow Disease and Humans What's Hot Christmas Disease Graves' Disease and Research Dystonia and Botox Injections Tourette Syndrome ... Ferraro Fighting Multiple Myeloma From Mary Kugler

4. Pediatric Database
   A definition of abetalipoproteinemia, followed by epidemiology, pathogenesis, clinical features, investigations and management.  
   http://www.icondata.com/health/pedbase/files/ABETALIP.HTM

5. Abetalipoproteinemia - Information / Diagnosis / Treatment / Prevention
   home neurological disorders brain diseases metabolic abetalipoproteinemiaabetalipoproteinemia. Information • Diagnosis • Treatment • Prevention.  
   http://www.healthcyclopedia.com/neurological-disorders/brain-diseases/metabolic/
   
   Extractions: Web Directory: Pediatric Database A definition of abetalipoproteinemia, followed by epidemiology, pathogenesis, clinical features, investigations and management. people involved in abetalipoproteinemia we are people who have this disorder annd /or family involved. group help with information, support and investigation

6. Abetalipoproteinemia Definition Of Abetalipoproteinemia. What Is Abetalipoprotei
   Definition of abetalipoproteinemia in the Dictionary and Thesaurus. Provides examplesfrom classic literature, search by definition of abetalipoproteinemia.  
   http://www.thefreedictionary.com/abetalipoproteinemia
   
   Extractions: Dictionaries: General Computing Medical Legal Encyclopedia Word: Word Starts with Ends with Definition Noun abetalipoproteinemia - a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels congenital disease genetic abnormality genetic defect genetic disease ... inherited disorder - a disease or disorder that is inherited genetically hypobetalipoproteinemia - a hereditary disorder characterized by low levels of beta-lipoproteins and lipids and cholesterol lipidosis - a disorder of lipid metabolism; abnormal levels of certain fats accumulate in the body Legend: Synonyms Related Words Antonyms Some words with "Abetalipoproteinemia" in the definition: acanthocytosis

7. THE MERCK MANUAL, Sec. 2, Ch. 16, Hypolipidemia And The Lipidoses
   syndromes. No treatment is required. abetalipoproteinemia (Acanthocytosis;BassenKornzweig Syndrome). A rare congenital disorder  
   http://www.merck.com/mrkshared/mmanual/section2/chapter16/16a.jsp

8. ClinicalTrials.gov - Information On Clinical Trials And Human Research Studies:
   Resources Help What's New About. Browse By Condition By Disease Heading Nervous System Diseases abetalipoproteinemia. Include trials that are no longer recruiting patients. 1 study was  
   http://clinicaltrials.gov/ct/screen/BrowseAny?path=/browse/by-condition/hier/BC1

9. OMIM - ABETALIPOPROTEINEMIA; ABL
   http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200100

10. ClinicalTrials.gov - Information On Clinical Trials And Human Research Studies:
    Resources Help What's New About. Browse By Condition By Disease Heading Blood and Lymph Conditions abetalipoproteinemia. Include trials that are no longer recruiting patients. 1 study  
    http://clinicaltrials.gov/ct/screen/BrowseAny?path=/browse/by-condition/hier/BC1

11. Entrez PubMed
    abetalipoproteinemia. New Terms abetalipoproteinemia*/diagnosis; abetalipoproteinemia*/etiology;abetalipoproteinemia*/metabolism;  
    http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

12. THE MERCK MANUAL, Sec. 2, Ch. 16, Hypolipidemia And The Lipidoses
    forms, most of the manifestations described for abetalipoproteinemia (see below) are applicable abetalipoproteinemia is caused by mutations in the gene for microsomal triglyceride  
    http://www.merck.com/pubs/mmanual/section2/chapter16/16a.htm
    
    Extractions: (Hypoproteinemia) Low lipoprotein levels in the plasma seen as rare familial disorders or secondary to hyperthyroidism, malabsorption, and malnutrition. Low levels of low density ( -) lipoproteins (LDL) can be seen in AIDS; hematologic malignancies, such as acute myelocytic leukemia and chronic myelocytic leukemia; and disorders with splenomegaly, such as Gaucher's disease. HYPOALPHALIPOPROTEINEMIA (Low HDL Levels) In many epidemiologic studies, low levels of high density ( -) lipoproteins (HDL) have been associated with increased coronary artery disease (CAD) risk. Low HDL levels often are due to genetic factors. Additionally, HDL levels are reduced by obesity, sedentary lifestyle, cigarette use, diabetes mellitus, uremia and nephrotic syndrome, and several drugs (thiazide diuretics, retinoids, -blockers, androgenic steroids, most progestational drugs, and probucol).

13. ORPHANET® : Abetalipoproteinemia
    ORPHANET. Orphanet database access. abetalipoproteinemia. Direct accessto data Summary Abetaliproteinemia is an autosomal recessive  
    http://www.orpha.net/static/GB/abetalipoproteinemia.html
    
    Extractions: Abetaliproteinemia is an autosomal recessive inherited inborn error of lipoprotein metabolism caused by mutation in a subunit of the microsomal trygliceride transfer protein (MTP), whose gene maps to chromosome 4q22-q24. This disease is very rare. Clinical features are malabsorption syndrome, pigmentary degeneration of the retina and progressive ataxic neuropathy. Red cells show a peculiar ``thorny'' deformation called acanthocytosis. The neurological symptoms are directly related to a deficiency of liposoluble vitamin E. Total cholesterol is low ( Clinical signs Update : 01/06/2004 Orphanet database access

14. ORPHANET® : Abetalipoproteinemia
    absorção/diarreia crónica; Alterações pigmentares periféricas da retina;  
    http://www.orpha.net/static/PT/abetalipoproteinemia.html

15. NeuroGate.com
    Global Search Add Url - Free Medline - Contact Us - Search. Copyright © 1998 byNeurogate.com. All rights reserved. Search results for "abetalipoproteinemia" NO MATCHES FOUND-Please select a different keyword or category OR. Search AltaVista for 'abetalipoproteinemia' Global Search  
    http://www.neurogate.com/neuro/result.php3?search=Abetalipoproteinemia&selec

16. ABETALIPOPROTEINEMIA - Meaning And Definition Of The Word
    Dictionary, Medical Dictionary. Search Dictionary abetalipoproteinemiaDictionary Entry and Meaning. WordNet Dictionary. Definition n a  
    http://www.hyperdictionary.com/dictionary/abetalipoproteinemia

17. Dorlands Medical Dictionary
    abetalipoproteinemia (abeta·lipo·pro·tein·emia) (aba²tschwa-lip²o-pro²te-ne¢me-schwa)an autosomal recessive disorder of lipoprotein metabolism in  
    http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

18. Abetalipoproteinemia
    Links to information and resources for abetalipoproteinemia, also known as BassenKornzweigsyndrome. abetalipoproteinemia (Chromosome 4) Guide picks.  
    http://rarediseases.about.com/cs/abetalipoproteinem/
    
    Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Home Essentials ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Abetalipoproteinemia (Chromosome 4)

19. ABETALIPOPROTEINEMIA
    abetalipoproteinemia A rare congenital disorder that causes the body to notproduce chylomicrons, low density lipoprotein (LDL), and very low density  
    http://www.medhelp.org/glossary2/new/gls_0036.htm
    
    Extractions: ABETALIPOPROTEINEMIA - A rare congenital disorder that causes the body to not produce chylomicrons low density lipoprotein LDL ), and very low density lipoprotein VLDL ). Individuals with this condition are unable to properly digest fats. Other findings include ataxia peripheral neuropathy , and other forms of nerve dysfunction. Treatment includes vitamin E

20. HealthCentral - General Encyclopedia - Bassen-Kornzweig Syndrome
    Alternative names abetalipoproteinemia Definition A rare, inherited diseasecharacterized by fatty stools and failure to thrive in infancy.  
    http://www.healthcentral.com/mhc/top/001666.cfm
    
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