MedlinePlus Medical Encyclopedia: Bassen-Kornzweig Syndrome bassenkornzweig syndrome. bassen-kornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. http://www.nlm.nih.gov/medlineplus/ency/article/001666.htm
Extractions: @import url(http://www.nlm.nih.gov/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 (
ABETALIPOPROTEINAEMIA (BASSEN-KORNZWEIG SYNDROME) Features Listed For ABETALIPOPROTEINAEMIA (bassenkornzweig syndrome) McKusick 200100. Pigmentary retinopathy/chorioretinitis. Ptosis of eyelids. Cholesterol/lipids, abnormal. Anaemia/red cell abnormalities. Muscle atrophy http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?6081
Disease - Bassen-Kornzweig Syndrome - Detroit, Michigan Disease bassen-kornzweig syndrome - courtesy of Henry Ford Health System of Detroit, Michigan Disease - bassen-kornzweig syndrome. Definition bassen-kornzweig syndrome is a rare, inherited http://www.henryfordhealth.org/12693.cfm
Extractions: Back to main Health Information page 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 And Risk: 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 Symptoms. Treatment. Prevention. bassenkornzweig syndrome. Alternative Names http://www.drkoop.com/ency/article/001666prv.htm
WebMD/Lycos A definition of bassenkornzweig syndrome, followed by a look at the alternate names, causes, symptoms, tests, treatment, prognosis and complications. http://webmd.lycos.com/content/asset/adam_disease_abetalipoproteinemia
Medical Encyclopedia: Bassen-Kornzweig Syndrome (Print Version) Medical Encyclopedia bassenkornzweig syndrome. URL of this page http//www.nlm.nih.gov/medlineplus/ency/article/001666.htm. Alternative names. http://www.nlm.nih.gov/medlineplus/print/ency/article/001666.htm
Extractions: To close this window, click on the "x" in the upper right hand corner of the window. URL of this page: http://www.nlm.nih.gov/medlineplus/ency/article/001666.htm 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. 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 Encyclopdia article about bassenkornzweig syndrome bassen-kornzweig syndrome. A Medical Encyclopedia Article provided by the University of Maryland with information on over 4000 medical topics including bassen-kornzweig syndrome http://www.umm.edu/medical-terms/04185.htm
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Bassen-Kornzweig Syndrome bassenkornzweig syndrome is a rare, inherited disease characterized by the inability to bassen-kornzweig syndrome is an autosomal recessive inherited disorder that affects both http://www.healthscout.com/ency/article/001666.htm
Extractions: Channels Home Today Women Men ... Drug Checker Advertisement Disease Injury 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 (
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► Bassen-Kornzweig Syndrome A medical encycopedia article on the topic bassen-kornzweig syndrome bassen-kornzweig syndrome is a rare, inherited disease characterized by the inability to bassen-kornzweig 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).
Extractions: Back Back to main Health Information page 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 And Risk: 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).
ENLmedical.com: Conditions And Concerns: Medical Encyclopedia: Bassen-Kornzweig A rare, inherited disease characterized by fatty stools and failure to thrive in infancy. Learn to make informed health care decisions with the Medical Encyclopedia at drkoop.com. bassenkornzweig syndrome. Causes and Risks bassen-kornzweig syndrome is an autosomal recessive http://www.enlmedical.com/article/001666.htm
Extractions: Bassen-Kornzweig syndrome is an autosomal recessive inherited disorder that affects both sexes, but predominantly males (70%). 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 - General Practice Notebook bassenkornzweig syndrome. Abetalipoproteinaemia is a disorder in the synthesis of serum lipoproteins containing apolipoprotein B http://www.gpnotebook.co.uk/cache/550502431.htm
Bassen-Kornzweig Syndrome - General Practice Notebook bassenkornzweig syndrome. Medical search. Abetalipoproteinaemia is a disorder in the synthesis of serum lipoproteins containing apolipoprotein http://www.gpnotebook.co.uk/medwebpage.cfm?ID=550502431
Extractions: 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).
