21. Abetalipoproteinemia - Wikipedia, The Free Encyclopedia abetalipoproteinemia is a rare genetic disorder that interferes with the normal Retrieved from http//en.wikipedia.org/wiki/abetalipoproteinemia http://en.wikipedia.org/wiki/Abetalipoproteinemia

Wikimedia needs your help in the final days of its fund drive. See our fundraising page Over US$225,000 has been donated since the drive began on 19 August. Thank you for your generosity! Abetalipoproteinemia From Wikipedia, the free encyclopedia. Abetalipoproteinemia is a rare genetic disorder that interferes with the normal absorption of fat and fat soluble vitamins from food. Contents Features Diagnosis Pathophysiology Treatment ... edit Features This disorder leads to a multiple vitamin deficiency, affecting the fat soluble vitamin A vitamin D vitamin E , and vitamin K . However, many of the observed effects are due to vitamin E deficiency in particular. edit Diagnosis The inability to absorb fat in the ileum will result in steatorrhea , or fat in the stool. As a result, this can be clinically diagnosed when foul smelling stool is encountered. Low plasma chylomicron levels are also characteristic. edit Pathophysiology Two genes have been identified in which mutations are associated with this disorder: microsomal triglyceride transfer protein (MTT) and apolipoprotein B (ApoB). There is an absence of betalipoprotein B. On intestinal

22. Definition Of Abetalipoproteinemia - WordReference.com Dictionary abetalipoproteinemia Definition from dictionary. Look up abetalipoproteinemia at MerriamWebster Look up abetalipoproteinemia at dictionary.com http://www.wordreference.com/definition/abetalipoproteinemia

Word Reference .com abetalipoproteinemia A 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 Category Tree: state condition status disorder ... hypobetalipoproteinemia abetalipoproteinemia Need more information? Ask a question in the forum. Look up "abetalipoproteinemia" at Merriam-Webster Look up "abetalipoproteinemia" at dictionary.com English Definition Home Suggestions Search Tips See Also: Aberdare Aberdeen Aberdonian aberrance ... abhorrent abetalipoproteinemia: in French in Italian in Spanish

23. Dr. Koop - Bassen-Kornzweig Syndrome abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency. Causes,incidence, and risk factors. BassenKornzweig syndrome is an autosomal recessive http://www.drkoop.com/ency/93/001666.html

Home Health Reference Bassen-Kornzweig syndrome Jul 29, 2005 Search: Dr.Koop MEDLINE Diseases Symptoms Procedures Natural Medicine ... Drug Library Inside DrKoop News Archive Animations Health Videos Health Tools ... Newsletters Bassen-Kornzweig syndrome Injury Disease Nutrition Poison ... Prevention Bassen-Kornzweig syndrome 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. Alternative Names: Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency 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 (

24. Abetalipoproteinemia abetalipoproteinemia. See Vitamin E. http://www.dietpower.com/help/diet/abetalipoproteinemia.htm

Abetalipoproteinemia See Vitamin E.

25. ► Bassen-Kornzweig Syndrome Alternative Names. abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency.Causes, incidence, and risk factors. BassenKornzweig syndrome is an http://www.umm.edu/ency/article/001666.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Disease Nutrition Surgery Symptoms Injury ... Encyclopedia (English) Toggle English Spanish Bassen-Kornzweig syndrome Overview Symptoms Treatment Prevention 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. Alternative Names: Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency 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). People with this disease are unable to properly digest fat, and have underdeveloped nerves (neuropathy), poor muscle coordination (

26. Bassen-Kornzweig Syndrome Medical Information Alternative Names. abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency.Causes. BassenKornzweig syndrome is an autosomal recessive inherited http://www.drugs.com/enc/bassen_kornzweig_syndrome.html

Home New Drugs Latest News Drug Interactions ... Forum Drugs.com - prescription drug and medicine information available on over 24,000 approved- medications and pharmaceuticals, including side effects and drug interactions. Log-in Register Advertisement Buy a Link Now Special Offers From our sponsors Categories Diabetes Gastro Center Weight Loss AIDS/HIV ... Sexual Health Advertisement Advanced Search Or click the first letter of a drug name: A B C D ... Z Bassen-Kornzweig syndrome Injury Disease Nutrition Poison ... Z Bassen-Kornzweig syndrome 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. Alternative Names Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency Causes 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 (

27. Netter Medical Illustrations - Search Results For Abetalipoproteinemia Netterimages.com The most trusted name in medical illustration PRICING ARTISTSREGISTER LOGIN. SEARCH RESULTS. 1 IMAGES IN SELECTION PAGE 1 OF 1 http://www.netterimages.com/image/list.htm?s=Abetalipoproteinemia

28. EMedicine - Vitamin E Deficiency : Article By Gary E Caplan, MD, MPH Severe deficiency, as may occur in persons with abetalipoproteinemia or fatmalabsorption, profoundly affects the central nervous system and can cause http://www.emedicine.com/med/topic2383.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Patient Education Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Medicine, Ob/Gyn, Psychiatry, and Surgery Endocrinology Vitamin E Deficiency Last Updated: March 5, 2004 Rate this Article Email to a Colleague Synonyms and related keywords: alpha tocopherol deficiency, alpha-tocopherol deficiency, tocopherol deficiency, vitamin deficiencies, antioxidant deficiency, abetalipoproteinemia, fat malabsorption, isolated vitamin E deficiency syndrome, malabsorption syndrome, cystic fibrosis, chronic cholestatic liver disease, short-bowel syndrome AUTHOR INFORMATION Section 1 of 11 Author Information Introduction Clinical Differentials ... Bibliography Author: Gary E Caplan, MD, MPH , Medical Director, Industrial Medical Group, University of Utah Rocky Mountain Center for Occupational and Environmen Coauthor(s): Terence Collins, MD, MPH, MPS , Chairman, Program Director, Professor, Department of Preventive Medicine and Environmental Health, University of Kentucky School of Public Health Gary E Caplan, MD, MPH, is a member of the following medical societies:

29. Bassen-Kornzweig Syndrome diarrhea,failure to thrive in infancy, and problems with nerves. Alternative Names.abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency http://www.lifespan.org/ADAM/English/HIE/001666.htm

Careers at Lifespan Volunteer your time Other ways to give Lifespan's A - Z Health Information Library Injury Disease Nutrition Poison ... Prevention Bassen-Kornzweig syndrome 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. Alternative Names Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency Causes 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). People with this disease are unable to properly digest fat, and have underdeveloped nerves (neuropathy), poor muscle coordination ( ataxia ), and other nerve disorders.

30. Birth Disorder Information Directory - A abetalipoproteinemia (Bassen Kornzweig Syndrome). List of Sites. Ablepharon.Ichthyosis Syndrome. Ablepharon-Ichthyosis. -Macrostomia Syndrome http://www.bdid.com/defectaa.htm

HOME Aa-Af Aagenaes Syndrome (Cholestasis-Lymphedema Syndrome) Cholestasis with lymphedema (Aagenaes syndrome) Aagenaes* Syndrom Aagenaes aagenaes syndrome ... Aagenaes* Syndrom Aarskog (Scott) Syndrome (Faciodigitogenital Syndrome, Faciogenital Dysplasia) List of Sites Aarskog-Like Syndrome (Faciodigitogenital Syndrome, Recessive Form; Teebi Naguib Alawadi Syndrome) Aarskog like syndrome FACIODIGITOGENITAL SYNDROME, RECESSIVE Aarskog Ose Pande Syndrome (Lipodystrophy Rieger Anomaly Diabetes) Aarskog ose pande syndrome LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES MELLITUS AASE Syndrome (Anemia with Triphalangeal Thumbs) List of Sites AASE Smith Syndrome (Hydrocephalus with Cleft Palate and Joint Contractures) AASE-Smith - Hydrocephalus; Cleft Palate; Joint Contractures AASE-SMITH SYNDROME AASE Smith Aase-Smith syndrome ABCD Syndrome (Albinism, Black Lock, Cell Migration Disorder of the Neurocytes of the Gut, and Deafness) abcd syndrome ABCD SYNDROME Abdallat Davis Farrage Syndrome (Neurocutaneous Syndrome, Abdallat Type; Spastic Paraplegia-Pigmentary Abnormalities) Abdallat (1980) - Neurocutaneous Syndrome SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES abdallat davis farrage syndrome abdallat davis farrage syndrome Abdominal Muscle Absence/Aplasia/Deficiency/Defect Anomalad/Syndrome See Prune Belly Syndrome Abetalipoproteinemia (Bassen Kornzweig Syndrome) List of Sites Ablepharon -Ichthyosis Syndrome Ablepharon-Ichthyosis -Macrostomia Syndrome Allison has AMS (Has a photo gallery)

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

HOME Abetalipoproteinemia (Bassen Kornzweig Syndrome) abetalipoproteinemia Abetalipoproteinaemia (Bassen-Kornzweig Syndrome) Abetalipoproteinemia abetalipoproteinemia ... HOME

32. PharmGKB: Abetalipoproteinemia abetalipoproteinemia. Alternate Names, abetalipoproteinemias; Apolipoprotein BDeficiency Disease; Bassen Kornzweig Disease; Bassen Kornzweig Syndrome; http://www.pharmgkb.org/do/serve?objId=PA443222&objCls=Disease

33. Oxidative Stress In Abetalipoproteinemia Patients Receiving Long-term Vitamin E Background Patients with abetalipoproteinemia develop progressive ataxic neuropathyand abetalipoproteinemia is a rare autosomal recessive disorder http://www.ajcn.org/cgi/content/full/79/2/226

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract Full Text (PDF) Purchase Article ... Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Request Permissions PubMed PubMed Citation Articles by Granot, E. Articles by Kohen, R. American Journal of Clinical Nutrition, Vol. 79, No. 2, 226-230, February 2004 American Society for Clinical Nutrition ORIGINAL RESEARCH COMMUNICATIONS Oxidative stress in abetalipoproteinemia patients receiving long-term vitamin E and vitamin A supplementation Esther Granot and Ron Kohen From the Department of Pediatrics, Hadassah University Hospital, Jerusalem (EG), and the Department of Pharmaceutics, School of Pharmacy, Hebrew University-Hadassah Medical School, Jerusalem (RK) Reprints not available. Address correspondence to E Granot, Department of Pediatrics, Hadassah University Hospital, PO Box 12000, Jerusalem, Israel. E-mail:

34. Oxidative Stress In Abetalipoproteinemia Patients Receiving Long-term Vitamin E Background Patients with abetalipoproteinemia develop progressive ataxic Key Words abetalipoproteinemia • oxidative stress • vitamin E • vitamin A http://www.ajcn.org/cgi/content/abstract/79/2/226

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Full Text Full Text (PDF) Purchase Article ... Citation Map Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager ... Request Permissions PubMed PubMed Citation Articles by Granot, E. Articles by Kohen, R. American Journal of Clinical Nutrition, Vol. 79, No. 2, 226-230, February 2004 American Society for Clinical Nutrition ORIGINAL RESEARCH COMMUNICATIONS Oxidative stress in abetalipoproteinemia patients receiving long-term vitamin E and vitamin A supplementation Esther Granot and Ron Kohen From the Department of Pediatrics, Hadassah University Hospital, Jerusalem (EG), and the Department of Pharmaceutics, School of Pharmacy, Hebrew University-Hadassah Medical School, Jerusalem (RK) Background: Patients with abetalipoproteinemia develop progressive ataxic neuropathy and retinopathy that are thought to be due, in part, to oxidative damage resulting from deficiencies of

35. AllRefer Health - Bassen-Kornzweig Syndrome (Abetalipoproteinemia, Acanthocytosi BassenKornzweig Syndrome (abetalipoproteinemia, Acanthocytosis, ApolipoproteinB Deficiency) information center covers causes, prevention, symptoms, http://health.allrefer.com/health/bassen-kornzweig-syndrome-info.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Bassen-Kornzweig Syndrome Bassen-Kornzweig Syndrome Definition Prevention Treatment Expectations or Prognosis ... Go To Main Page Alternate 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 (

36. AllRefer Health - Bassen-Kornzweig Syndrome Prevention (Abetalipoproteinemia, Ac BassenKornzweig Syndrome (abetalipoproteinemia, Acanthocytosis, ApolipoproteinB Deficiency) information center covers Prevention. http://health.allrefer.com/health/bassen-kornzweig-syndrome-prevention.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Bassen-Kornzweig Syndrome : Prevention of Bassen-Kornzweig Syndrome Bassen-Kornzweig Syndrome Definition Prevention Treatment Expectations or Prognosis Complications Calling Your Health Care Provider ... Go To Main Page Alternate Names : Abetalipoproteinemia, Acanthocytosis, Apolipoprotein B Deficiency Prevention High doses of fat soluble vitamins may be able to slow progression of some problems such as degeneration of the retina and decreased vision. Previous Top Next Jump to another section Definition Prevention Treatment Prognosis Complications Calling Your Health Care Provider Topics that might be of interest to you Failure to Thrive CBC LDL Triglyceride Level ... VLDL Other Topics Blindness Cholesterol Fat Movement - Uncoordinated ... Vitamin K Review Date : 8/6/2003 Reviewed By : Douglas R. Stewart, M.D., Division of Medical Genetics, Hospital of the University of Pennsylvania, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

37. Abetalipoproteinemia abetalipoproteinemia. Used for. acanthocytosis. Used for. Bassen Kornzweigsyndrome. Used for. betalipoprotein deficiency disease. Used for http://crisp.cit.nih.gov/Thesaurus/00000005.htm

Prev Term: Abelson's virus Next Term: abnormal cardiovascular bypass abetalipoproteinemia Used for: acanthocytosis Used for: Bassen Kornzweig syndrome Used for: betalipoprotein deficiency disease Used for: hypobetalipoproteinemia Used for: microsomal triglyceride transfer protein deficiency disease Broader Terms: familial hypolipoproteinemia Related Terms: autosomal recessive trait Scope Note: disorder of lipid metabolism inherited as an autosomal recessive trait characterized by the near absence of apolipoprotein B and apoB containing lipoproteins in plasma; microsomal triglyceride transfer protein is deficient or absent in enterocytes; clinical and laboratory findings include acanthocytosis, hypocholesterolemia, peripheral neuropathy, posterior column degeneration, ataxia, and steatorrhea; intellectual abilities may also be impaired. Term Number: Send your comments to: Melody Lowe

38. MedlinePlus Medical Encyclopedia: Bassen-Kornzweig Syndrome abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency. Definition Returnto top. BassenKornzweig syndrome is a rare, inherited disease http://www.nlm.nih.gov/medlineplus/ency/article/001666.htm

@import url(/medlineplus/images/advanced.css); Skip navigation Medical Encyclopedia Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Bassen-Kornzweig syndrome Contents of this page: Alternative names Definition Causes, incidence, and risk factors Symptoms ... Prevention Alternative names Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency Definition Return to top 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. Causes, incidence, and risk factors Return to top 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 (

39. Www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Abetalipop MTHICD9/ET/272.5 MTH/PT/U000241 DXP/DI/U000001 CSP/PT/18495137 http://www.nlm.nih.gov/cgi/mesh/2K/MB_cgi?term=Abetalipoproteinemia

40. Arch Ophthalmol -- Helicoid Peripapillary Chorioretinal Degeneration In Abetalip We report a case of HPCD associated with abetalipoproteinemia. Report of a CaseA 24year-old woman had been diagnosed with abetalipoproteinemia at age 2 http://archopht.ama-assn.org/cgi/content/extract/116/2/250

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA (1998-2004) JAMA CareerNet For The Media Meetings Peer Review Congress Vol. 116 No. 2, February 1998 Featured Link E-mail Alerts Case Reports and Small Case Series Article Options Full text PDF Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Wong AM Heon E Articles that cite this article ISI Web of Science (2) ... Contact me when this article is cited Helicoid Peripapillary Chorioretinal Degeneration in Abetalipoproteinemia Arch Ophthalmol. Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. Abetalipoproteinemia is a rare autosomal recessive disorder characterized by the absence of apolipoprotein B. It is caused by mutations of the microsomal triglyceride-transfer protein gene.

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