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

61. Prep For USMLE Step 1 » Abetalipoproteinemia
abetalipoproteinemia Can anybody tell me etilogy,sign and symptoms and treatmentfor abetalipoproteinemia . thanks in advance. Re abetalipoproteinemia
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Abetalipoproteinemia

Author Message asmi
Posts: 3845

Abetalipoproteinemia Can anybody tell me etilogy,sign and symptoms and treatment for abetalipoproteinemia .
thanks in advance
Cool Surfer
Posts: 61

Re: Abetalipoproteinemia Hi i found this for you from harrisons textbook of medicine.
Hope it helps you. This chapter focuses on the major lipid disorders, including both the dyslipoproteinemias caused by single-gene defects and the disorders that are likely to be multifactorial in origin. A practical approach is provided to assist in the identification, evaluation, and treatment of patients with increased risk of CHD. LIPID AND LIPOPROTEIN TRANSPORT LIPOPROTEIN STRUCTURE Lipoproteins have been classified on the basis of their densities into five major classes:(1) chylomicrons, (2) very low density lipoproteins (VLDL), (3) intermediate-density lipoproteins (IDL), (4) LDL, and (5) high-density lipoproteins (HDL). APOLIPOPROTEINS The apolipoproteins (apos) provide structural stability to the lipoproteins and determine the metabolic fate of the particles upon which they reside. There are two forms of apo B¾apo B100 and apo B48. Apo B100 is the major apolipoprotein of VLDL, IDL, and LDL, comprising approximately 30, 60, and 95% of the protein in these lipoproteins, respectively. Apo B100 has a molecular mass of about 545 kDa and is synthesized in the liver. It is essential for the assembly and secretion of VLDL from the liver and is the ligand for the removal of LDL by the LDL receptor. The LDL receptor is a cell-surface protein that binds and internalizes lipoproteins that contain apo B100 or apo E. The LDL receptor binding domain of apo B100 is the sequence between amino acids 3200 and 3600, a region that is absent in apo B48.

62. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/Neurological_Disor
News about abetalipoproteinemia More news about abetalipoproteinemia . Booksabout abetalipoproteinemia More books about abetalipoproteinemia .
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Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Metabolic Abetalipoproteinemia (3 links) See Also: News about Abetalipoproteinemia [ More news about Abetalipoproteinemia Books about Abetalipoproteinemia [ More books about Abetalipoproteinemia Links about Abetalipoproteinemia
  • Pediatric Database - A definition of abetalipoproteinemia, followed by epidemiology, pathogenesis, clinical features, investigations and management. WebMD/Lycos - A definition of Bassen-Kornzweig syndrome, followed by a look at the alternate names, causes, symptoms, tests, treatment, prognosis and complications.

63. Abetalipoproteinemia
abetalipoproteinemia. Individuals with abetalipoproteinemia may be prescribedspecial vitamin E supplements by a physician to treat this disorder.
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Abetalipoproteinemia
Abetalipoproteinemia is a rare inherited disorder of fat metabolism that results in poor absorption of dietary fat and vitamin E . The vitamin E deficiency associated with this disease causes problems such as poor transmission of nerve impulses, muscle weakness, and degeneration of the retina that can cause blindness . Individuals with abetalipoproteinemia may be prescribed special vitamin E supplements by a physician to treat this disorder. This article is a stub. You can help Wikipedia by expanding it.

64. Abetalipoproteinemia
The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set.
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65. SearchBug Directory: Health: Conditions_and_Diseases: Neurological_Disorders: Br
Search the Web Web. Open Directory. Search abetalipoproteinemia,
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Web Pages - ranked by popularity people involved in abetalipoproteinemia http://groups.yahoo.com/group/Abetalipoproteinemia/ we are people who have this disorder annd /or family involved. group help with information, support and investigation Pediatric Database http://www.icondata.com/health/pedbase/files/ABETALIP.HTM A definition of abetalipoproteinemia, followed by epidemiology, pathogenesis, clinical features, investigations and management. WebMD/Lycos http://webmd.lycos.com/content/asset/adam_disease_abetalipoproteinemia A definition of Bassen-Kornzweig syndrome, followed by a look at the alternate names, causes, symptoms, tests, treatment, prognosis and complications.
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66. Conditions And Diseases: Neurological Disorders: Brain Diseases: Metabolic: Abet
Information on Conditions and Diseases, Neurological Disorders, Brain Diseases,Metabolic, abetalipoproteinemia and much more Treasure Coast Health.
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68. Abetalipoproteinemia From Linkspider UK Health Directory
abetalipoproteinemia by Linkspider UK, abetalipoproteinemia links andabetalipoproteinemia topics from our Health directory. Helping
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69. 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
Abetalipoproteinemia resources. Information for medical researchers, health professionals, bioscientists, and policy makers.
Recommended References. [see index for total category]
KEY ABSTRACTS:
PUBMED Citations:
Innovations and emerging technologies in Abetalipoproteinemia, Patent List (when available) for Abetalipoproteinemia:

6,465,230: 27411, a novel human PGP synthase
6,444,802: Human aminopeptidase
6,403,358: 21529, a novel adenylate cyclase
6,387,638: Heregulin variants
6,369,075: 7[4'-trifluoromethyl-biphenyl-2-carbonyl)amino]-quinoline-3-carboxylic acid amides, and method of inhibiting the secretion of apolipoprotein B
6,365,373: Nucleic acids encoding NGF variants 6,337,187: 18891, a novel human lipase 6,333,310: NGF variants 6,313,169: Lutein esters having high bioavailability 6,288,234: Multibinding inhibitors of microsomal triglyceride transferase protein 6,287,765: Methods for detecting and identifying single molecules 6,281,228: Heterocyclic inhibitors of microsomal triglyceride transfer protein and method 6,280,732: Methods of using an AL-1 neurotrophic factor immunoadhesin

70. Acanthocytes - Abetalipoproteinemia
Acanthocytes abetalipoproteinemia. The term acanthocyfe was applied in1952 to the red cell form seen in hereditary abetalipoproteinemia.
http://www.academic.marist.edu/~jzmz/topics/description_rbc/description33.html
Acanthocytes - abetalipoproteinemia
A form of spicule formation is the acanthocyte or thorny cell. One is seen in this slide near the center of the field. Morphologically, acanthocytes differ from burr cells in that they are spherocytes with thorns, darkly stained, and have no central pallor. The term acanthocyfe was applied in 1952 to the red cell form seen in hereditary abetalipoproteinemia. The blood shown here is from such a patient. Abetalipoproteinemia is a rare syndrome thought to be inherited from both parents as an autosomal recessive trait. Acan~ thocytes are seen commonly in liver disease, especially Laennec',C cirrhosis. They are found in small numbers in acquired hypobetali poproteinemia associated with malabsorotion, hemolytic anemia, and after the administration of heparin.

71. GeneCards Disorder Information: Abetalipoproteinemia
GeneCards Disorder Information abetalipoproteinemia. Search different databasescontaining disease information by clicking on the buttons below.
http://www.rzpd.de/cgi-bin/cards/disodisp?Abetalipoproteinemia

72. Abetalipoproteinemia : On Medical Dictionary Online
Apolipoprotein B deficiency. Causes And Risk. BassenKornzweig
http://www.online-medical-dictionary.org/?q=Abetalipoproteinemia

73. Wuup.de - /Health/Conditions_and_Diseases/Neurological_Disorders
Translate this page abetalipoproteinemia. Siehe auch people involved in abetalipoproteinemia- we are people who have this disorder annd /or family involved.
http://wuup.de/index.php/Health/Conditions_and_Diseases/Neurological_Disorders/B

74. ACR Learning File Web
Click here for ordering information. Diagnosis abetalipoproteinemia. Returnto top. Copyright © 1994 2002 American College of Radiology.
http://www.learningfile.com/learning_file/viewcase.php?section=pd&case_num=3102

75. Directorio De Calidad De Vida | Lasalud.com
Translate this page Se han encontrado 97 resultados para abetalipoproteinemia. 1, Dorlands Medical Dictionary. abetalipoproteinemia, a variant of abetalipoproteinemia in which
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76. Directorio De Tratamiento | Lasalud.com
Translate this page Se han encontrado 46 resultados para abetalipoproteinemia. of neuropathyand retinopathy associated with abetalipoproteinemia and cystic
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77. A-Beta-Lipoproteinemia,Bassen-Kornzweig Syndrome,Betalipoprotein Deficiency,A-Be
(as defined at http//rarediseases.about.com/library/weekly/aa072601a.htm).abetalipoproteinemia Problem with using fat in the body.
http://www.icomm.ca/geneinfo/abl.htm
A-Beta-Lipoproteinemia,Bassen-Kornzweig Syndrome,Betalipoprotein Deficiency,A-Beta-Lipoproteinemia,Bassen-Kornzweig Syndrome,Betalipoprotein Deficiency,Acanthocytosis Bassen-Kornzweig Syndrome,Low-Density Beta Lipoprotein Deficiency
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DISORDERS GLOSSARY A-Beta-Lipoproteinemia
also known as:
Bassen-Kornzweig Syndrome
Betalipoprotein Deficiency
Acanthocytosis
(as defined by the
National Organization for Rare Disorders
Acanthocytosis is a digestive disorder that is characterized by the absence of very low density lipoproteins (VLDL) and chylomicrons in the plasma. Chylomicrons are very small fatty droplets that are covered with a beta-lipoprotein and perform an essential function in fat transport in the blood and, thus, in fat metabolism. The absense of VLDL and of chylomicrons interferes with the absorption of fat and leads to excessive fats excretion (steatorrhea). Other symptoms include abnormal red blood cells (acanthocytes), a vision disorder (retinitis pigmentosa), and impaired muscle coordination (ataxia).

78. Medical Encyclopedia
abetalipoproteinemia, acanthocytosis, apolipoprotein, blood, care, causes, chain,complications, coordination, deficiency, definition, dietary, disease
http://www.georgetownuniversityhospital.org/body.cfm?id=18&action=display&articl

79. Abetalipoproteinemia - Wikipedia En Español
Metabolic AtaxiasMETABOLIC ATAXIAS.
http://es.wikipedia.org/wiki/Abetalipoproteinemia
Abetalipoproteinemia
De Wikipedia, la enciclopedia libre.
Sinónimos: Síndrome de Bassen Kornzweig , Síndrome de Lipoproteína Beta de Baja Densidad. Código CIE-9-MC: 272.5 La abetalipoproteinemia enfermedad del tubo digestivo que se caracteriza por la ausencia de lipoproteínas de muy baja densidad (VLDL) y de quilomicrones en el plasma, mala absorción de la grasa produciendo una esteatorrea (excreción excesiva de grasas en las heces). Se acompaña de: acantocitosis (glóbulos rojos en la sangre anormales, con aspecto espinoso), retinitis pigmentaria (trastorno de la visión que se produce por una degeneración de la retina), y ataxia (alteración de la capacidad de coordinar los movimientos. Views Herramientas personales Navegación Buscar Herramientas Otros idiomas

80. MeSH-D Terms Associated To MeSH-C Term Abetalipoproteinemia
MeSHD terms associated to MeSH-C term abetalipoproteinemia, G2D Home.The number indicates the strength of the association of the
http://www.bork.embl-heidelberg.de/g2d/c2d.pl?Abetalipoproteinemia:unknown

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