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

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

3. ABETALIPOPROTEINEMIA
   A brief definition of abetalipoproteinemia.Category Health Conditions and Diseases abetalipoproteinemiaabetalipoproteinemia A rare congenital disorder that causes the body to notproduce chylomicrons, low density lipoprotein (LDL), and very low density  
   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

4. Abetalipoproteinemia
   Feature article on abetalipoproteinemia, dated 7/26/01. What is it? abetalipoproteinemia (also known as BassenKornzweig syndrome) is an inherited disorder that affects how  
   http://rarediseases.about.com/library/weekly/aa072601a.htm
   
   Extractions: Abetalipoproteinemia (also known as Bassen-Kornzweig syndrome) is an inherited disorder that affects how fats are made and used in the body. The body needs fats for healthy nerves, muscles, and digestion. Like oil and water, fats can't travel in the blood around the body by themselves-they just don't mix in. Fats attach to special proteins called lipoproteins to travel to wherever they're needed. Because of a genetic disorder, people with abetalipoproteinemia don't produce a critical "building block" (a special protein) for making lipoproteins. Without enough lipoproteins, fats can't be digested properly or travel around the body to where they're needed, which leads to serious health problems.

5. Abetalipoproteinemia
   Links to information and resources for abetalipoproteinemia, also known as BassenKornzweigsyndrome. abetalipoproteinemia (Chromosome 4) Guide picks.  
   http://rarediseases.about.com/cs/abetalipoproteinem/

6. Med Help
   A brief definition of abetalipoproteinemia.  
   http://medhlp.netusa.net/glossary/new/GLS_0033.HTM

7. ORPHANET® : Abetalipoproteinemia
   Translate this page ORPHANET. ORPHANET database access. abetalipoproteinemia. Directaccess to details Alias Bassen-Kornzweig disease. Home Page.  
   http://www.orpha.net/static/GB/abetalipoproteinemia.html

8. Katalog - Wirtualna Polska
   Serwis Katalog w Wirtualna Polska S.A. pierwszy portal w Polsce.  
   http://katalog.wp.pl/DMOZ/Health/Conditions_and_Diseases/Neurological_Disorders/

9. Service Page - Pathologie Information
   DISEASE abetalipoproteinemia, Synonym(s) BassenKornzweig disease,CIM E78.6, abetalipoproteinemia, Bassen Kronsweig Disease.  
   http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=GB&Expert=14

10. Abetalipoproteinemia
    Medical Encyclopdia article about abetalipoproteinemia A resource with information on over 4000 medical topics including abetalipoproteinemia  
    http://www.marylandadd.com/medical-terms/04182.htm

11. SISTEMA DE INFORMACION SOBRE ENFERMEDADES RARAS EN ESPAÑOL (SIERE)
    Translate this page La abetalipoproteinemia es una enfermedad del tubo digestivo que se caracterizapor la ausencia de lipoproteínas de muy baja densidad (VLDL) y de  
    http://cisat.isciii.es/er/prg/er_bus2.asp?cod_enf=6

12. Abetalipoproteinemia
    rare, autosomal recessive malabsorption of fat progressive neurologic deterioration In GI tract © 2002, C.E.  
    http://chorus.rad.mcw.edu/to-go/00432.html

13. Abetalipoproteinemia (Bassen Kornzweig Syndrome)
    Abetalipoproteinaemia (Bassen-Kornzweig Syndrome); abetalipoproteinemia;  
    http://www.bdid.com/abetalipoproteinemia.htm

14. Birth Disorder Information Directory - A
    Deficiency/Defect Anomalad/Syndrome See Prune Belly Syndrome. abetalipoproteinemia(Bassen Kornzweig Syndrome) List of Sites. Ablepharon  
    http://www.bdid.com/defectaa.htm
    
    Extractions: HOME Aagenaes Syndrome (Cholestasis-Lymphedema Syndrome) Aarskog (Scott) Syndrome (Faciodigitogenital Syndrome, Faciogenital Dysplasia) Aarskog-Like Syndrome (Faciodigitogenital Syndrome, Recessive Form; Teebi Naguib Alawadi Syndrome) Aarskog Ose Pande Syndrome (Lipodystrophy Rieger Anomaly Diabetes) AASE Syndrome (Anemia with Triphalangeal Thumbs) AASE Smith Syndrome (Hydrocephalus with Cleft Palate and Joint Contractures) ABCD Syndrome (Albinism, Black Lock, Cell Migration Disorder of the Neurocytes of the Gut, and Deafness) Abdallat Davis Farrage Syndrome (Neurocutaneous Syndrome, Abdallat Type; Spastic Paraplegia-Pigmentary Abnormalities) Abdominal Muscle Absence/Aplasia/Deficiency/Defect Anomalad/Syndrome Abetalipoproteinemia (Bassen Kornzweig Syndrome) Ablepharon -Macrostomia Syndrome Allison has AMS (Has a photo gallery)

15. 1Up Health > Health Links Directory > Conditions And Diseases: Neurological Diso
    Conditions and Diseases Neurological Disorders Brain Diseases Metabolic abetalipoproteinemia. Med Help A brief definition of abetalipoproteinemia.  
    http://www.1uphealth.com/links/metabolic-abetalipoproteinemia.html

16. 1Up Health > Bassen-Kornzweig Syndrome > Causes, Incidence, And Risk Factors Of
    Comprehesive information on BassenKornzweig syndrome (abetalipoproteinemia,Acanthocytosis, Apolipoprotein B deficiency). Covers  
    http://www.1uphealth.com/health/bassen_kornzweig_syndrome_info.html
    
    Extractions: 1Up Health Bassen-Kornzweig syndrome Alternative Medicine Clinical Trials ... Health Topics A-Z Search 1Up Health Bassen-Kornzweig syndrome Information Bassen-Kornzweig syndrome Causes, Incidence, and Risk Factors Alternative names : Abetalipoproteinemia, Acanthocytosis, Apolipoprotein B deficiency Definition : Bassen-Kornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. It results in fatty stools, diarrhea, failure to thrive in infancy, and problems with nerves. Bassen-Kornzweig syndrome is an autosomal recessive inherited disorder that affects both sexes, but predominantly males (70%). It is due to mutations in one of two genes: apolipoprotein B (APOB) or microsomal triglyceride transfer protein (MTP). The syndrome causes the body not to make lipoproteins (molecules of fat combined with protein ) including low-density lipoproteins ( LDL ), very-low-density lipoproteins ( VLDL ), and chylomicrons (small molecules of fat in the blood).

17. Abetalipoproteinemia - AnsMe.com Dictionary (define)
    Similar pages Genetic disorder and birth defectsaarskog,aase-smith, Links to genetic support groups and information pages for genetic disorders andbirth defects,aarskog,aase-smith,abetalipoproteinemia,abdominal muscle  
    http://define.ansme.com/words/a/abetalipoproteinemia.html

18. IComm: File Not Found!
    BassenKornzweig Syndrome ..abetalipoproteinemia). NationalTay-Sachs and Allied Diseases Association http//www.ntsad.org  
    http://www.icomm.ca/geneinfo/b.htm

19. Bassen-Kornzweig Syndrome
    nerves. Alternative Names abetalipoproteinemia; Acanthocytosis; ApolipoproteinB deficiency. Causes, incidence, and risk factors  
    http://www.pennhealth.com/ency/article/001666.htm
    
    Extractions: Causes, incidence, and risk factors: Bassen-Kornzweig syndrome is an autosomal recessive inherited disorder that affects both sexes, but predominantly males (70%). It is due to mutations in one of two genes: apolipoprotein B (APOB) or microsomal triglyceride transfer protein (MTP). The syndrome causes the body not to make lipoproteins (molecules of fat combined with protein ) including low-density lipoproteins ( LDL ), very-low-density lipoproteins ( VLDL ), and chylomicrons (small molecules of fat in the blood).

20. Abetalipoproteinemia Resource Updates
    abetalipoproteinemia resources. Other forms are much less frequent, andinclude ataxia with vitamin E deficiency, abetalipoproteinemia.  
    http://www.health.xq23.com/inst/Research_Updates/Abetalipoproteinemia.html

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