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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

21. Abetalipoproteinemia - Wikipedia, The Free Encyclopedia
Open Directory Health Conditions and Diseases Neurological Pediatric Database - A definition of abetalipoproteinemia, followed by epidemiology,pathogenesis, clinical features, investigations and management.
http://en.wikipedia.org/wiki/Abetalipoproteinemia
Abetalipoproteinemia
From Wikipedia, the free encyclopedia.
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 Views Personal tools Navigation Search Toolbox

22. Abetalipoproteinemia
abetalipoproteinemia. abetalipoproteinemia is a rare inherited disorder of fatmetabolism that results in poor absorption of dietary fat and vitamin E.
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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 from Wikipedia . All text is available under the terms of the GNU Free Documentation License

23. Online Encyclopedia - Abetalipoproteinemia
, Encyclopedia Entry for abetalipoproteinemia.Dictionary Definition of abetalipoproteinemia. abetalipoproteinemia......Encyclopedia
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Encyclopedia Entry for Abetalipoproteinemia
Dictionary Definition of 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 Home Alphabetical Index See our sister sites: Find a Resume Diplomat City Your Quotations Your Lookup ... Your Dogs Content on this site is provided for informational purposes only. We do not accept responsibility for any loss, injury or inconvenience sustained by any person resulting from information published on this site.
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24. Abetalipoproteinemia
Terms of Use. abetalipoproteinemia. Definition abetalipoproteinemia. abetalipoproteinemia.Noun. All rights reserved. Crosswords abetalipoproteinemia.
http://www.websters-online-dictionary.org/definition/english/ab/abetalipoprotein
Philip M. Parker, INSEAD.
Abetalipoproteinemia
Definition: Abetalipoproteinemia
Abetalipoproteinemia
Noun
. 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. Source: WordNet 1.7.1
Crosswords: Abetalipoproteinemia
English words defined with "abetalipoproteinemia" acanthocytosis references Specialty definitions using "abetalipoproteinemia" Apolipoproteins B references Top
Specialty Definition: Abetalipoproteinemia
(From Wikipedia , the free Encyclopedia) 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.
Source: adapted by the editor from Wikipedia , the free encyclopedia under a copyleft GNU Free Documentation License (GFDL) from the article " Abetalipoproteinemia Top
Frequency of Internet Keywords: Abetalipoproteinemia
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25. Abetalipoproteinemia
abetalipoproteinemia Ciencia.net - Noticias científicas - abetalipoproteinemia .
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abetalipoproteinemia
English Translation: abetalipoproteinemia
Language Expression English Translation or Definition Italian abetalipoproteinemia abetalipoproteinemia Spanish abetalipoproteinemia abetalipoproteinemia Source: compiled by the editor from the definition of abetalipoproteinemia ; see credits. Top
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26. Glosario_Abetalipoproteinemia
Translate this page A B C D E F G H I J K L LL M N Ñ O P Q R S T U V W X Y Z. DATOS SOLICITADOS( A ), Término abetalipoproteinemia. Definición La
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27. SIERE (Sistema De Información Sobre Enfermedades Raras En Español)
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
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28. Abetalipoproteinemia
Translate this page abetalipoproteinemia Sinónimos Síndrome de Bassen Kornzweig, Síndromede Lipoproteína Beta de Baja Densidad. Código CIE-9-MC 272.5.
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Abetalipoproteinemia
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.
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29. Neurological Disorders, Brain Diseases, Metabolic, Abetalipoproteinemia
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  • 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

30. Abetalipoproteinemia - Dictionary Definition
Dictionary Definition of abetalipoproteinemia. Click Here, The noun abetalipoproteinemia has 1 senses.
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Dictionary Definition of abetalipoproteinemia
The noun "abetalipoproteinemia" has 1 senses. 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
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  • 31. Vitamin E (associated With Abetalipoproteinemia)
    You are here Health Concerns / Diabetes / Vitamin E (associated with abetalipoproteinemia)/. Vitamin E (associated with abetalipoproteinemia).
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    32. Health Topics
    nerves. Alternative Names abetalipoproteinemia; Acanthocytosis; ApolipoproteinB deficiency. Causes, incidence, and risk factors
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    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 ( 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.

    33. Abetalipoproteinemia - BlueRider.com
    abetalipoproteinemia. Your search results search for abetalipoproteinemia on Google abetalipoproteinemia n. 1), a rare
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    abetalipoproteinemia [n] 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 Synonyms: See Also: hypobetalipoproteinemia lipidosis
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    34. Gimenei >> Health >> Conditions_and_Diseases >> Neurological_Disorders >> Brain_
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    35. Síndrome De Bassen-Kornzweig - Información General
    Translate this page Nombres alternativos abetalipoproteinemia. Definición Es una raraenfermedad congénita, caracterizada por heces grasosas y retraso
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    Síndrome de Bassen-Kornzweig - Información general
    Información general Síntomas Tratamiento
    Nombres alternativos:
    Abetalipoproteinemia.
    Definición:
    Es una rara enfermedad congénita, caracterizada por heces grasosas y retraso en el desarrollo infantil.
    Causas, incidencia y factores de riesgo:
    El síndrome de Bassen-Kornzweig es un trastorno congénito raro, que suele transmitirse con carácter autosómico recesivo. A pesar de que el síndrome afecta ambos sexos, predomina en los hombres (70% de los casos). La alteración radica en la incapacidad del organismo para producir lipoproteínas (moléculas de grasa combinadas con proteína ) de los tipos LDL , lipoproteínas de baja densidad y lipoproteínas de muy baja densidad ( VLDL ) y quilomicrones (pequeñas moléculas de grasa presentes en la sangre). Estas sustancias son indispensables para la absorción de grasas. Las personas con este síndrome presentan deterioro en la digestión de este tipo de nutrientes, lo que conduce al desarrollo insuficiente e inapropiado de los nervios (neuropatía), mala coordinación muscular ataxia ) y otros trastornos nerviosos.

    36. Tropes
    obesitymetabolic syndrome (2) AOMS1, SYNX 605552 3q27 Abdominal obesity-metabolicsyndrome, 605552 (2) AOMS2 605572 17p12 abetalipoproteinemia (3) APOB , FLDB
    http://freesense.free.fr/Diseases/d/0009.htm

    http://www.ncbi.nlm.nih.gov/htbin-post/Omim/getmorbid
    obesity -metabolic syndrome (2) AOMS1, SYNX 605552 3q27 Abdominal obesity -metabolic syndrome, 605552 (2) AOMS2 605572 17p12 Abetalipoproteinemia (3) APOB , FLDB 107730 2p24 Abetalipoproteinemia Precedent Suivant Tropes Web V1.0

    37. Brain Diseases, Metabolic, Inborn
    obesitymetabolic syndrome (2) AOMS1, SYNX 605552 3q27 Abdominal obesity-metabolicsyndrome, 605552 (2) AOMS2 605572 17p12 abetalipoproteinemia (3) APOB.
    http://freesense.free.fr/Diseases/c/404.htm

    http://www.ncbi.nlm.nih.gov/htbin-post/Omim/getmorbid
    , AAS 305400 Xp11. 21 Abdominal obesity -metabolic syndrome (2) AOMS1, SYNX 605552 3q27 Abdominal obesity -metabolic syndrome, 605552 (2) AOMS2 605572 17p12 Abetalipoproteinemia (3) APOB , FLDB 107730 2p24 Abetalipoproteinemia , 200100 (3) MTP 157147 4q22-q24 Acampomelic campolelic dysplasia (3) SOX9, CMD1, SRA1
    http://www.ncbi.nlm.nih.gov/genome/guide/HsChrX.shtml
    Clusters Mouse Homologies for Human Chr. X_chromosome X Disease Genes Myelin stained section of brain in adrenoleukodystrophy Adrenoleukodystrophy Duchenne Muscular_dystrophy Lowe Syndrome Norrie Disease Rett_syndrome See OMIM or Genes and Disease for additional examples
    http://www.ncbi.nlm.nih.gov/genome/guide/HsChr1.shtml
    for Human Chr. 1 Chromosome 1 Disease Genes Some diseases associated with chromosome 1 mutations Chediak-higashi_syndrome Charcot-Marie-Tooth Neuropathy-2a Ductal Breast_cancer Usher Syndrome,
    http://www.ncbi.nlm.nih.gov/disease/Metabolism.html
    Metabolism Adrenoleukodystrophy Atherosclerosis Best disease Glucose galactose malabsorption Gyrate_atrophy Juvenile onset diabetes Obesity Paroxysmal nocturnal hemoglobinuria Phenylketonuria Tay-sachs_disease METABOLISM is the means by
    http://www.ncbi.nlm.nih.gov/genome/guide/HsChr15.shtml

    38. Health - Conditions And Diseases - Neurological Disorders - Brain
    Top Health Conditions and Diseases Neurological Disorders Brain DiseasesMetabolic abetalipoproteinemia See also Health Conditions
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    39. :: Ez2Find :: Abetalipoproteinemia
    Guide abetalipoproteinemia, Global Metasearch Any Language Guides, abetalipoproteinemia.ez2Find Home Directory Health Conditions
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    40. Startplane /Health/Conditions_and_Diseases/Neurological_Disorders/Brain_Diseases
    abetalipoproteinemia. See also people involved in abetalipoproteinemia we are people who have this disorder annd /or family involved.
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    See also: Links
    • 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. people involved in abetalipoproteinemia - we are people who have this disorder annd /or family involved. group help with information, support and investigation
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