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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

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

Extractions: Over US$225,000 has been donated since the drive began on 19 August. Thank you for your generosity! Abetalipoproteinemia is a rare genetic disorder that interferes with the normal absorption of fat and fat soluble vitamins from food. edit 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 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 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
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
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

Extractions: Inside DrKoop News Archive Animations Health Videos Health Tools ... Newsletters Injury Disease Nutrition Poison ... 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. 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 (
Abetalipoproteinemia
abetalipoproteinemia. See Vitamin E.
http://www.dietpower.com/help/diet/abetalipoproteinemia.htm
► 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

Extractions: Toggle English Spanish 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. 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).
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

Extractions: Advanced Search Or click the first letter of a drug name: A B C D ... Z Injury Disease Nutrition Poison ... Z 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. Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency 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 (
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
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

Extractions: (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 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:
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

Extractions: Other ways to give Injury Disease Nutrition Poison ... Prevention 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. Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency 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).
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

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

Extractions: 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 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:
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

Extractions: 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 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
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

Extractions: 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 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 (
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

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

Extractions: @import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: 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 (
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
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

Extractions: 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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