MedlinePlus Medical Encyclopedia: Bassen-Kornzweig Syndrome bassenkornzweig 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(/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 (
Bassen-Kornzweig Syndrome bassenkornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. It results in http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
MedlinePlus Medical Encyclopedia: Topics Beginning With A-Ag Abetalipoproteinemia see bassenkornzweig syndrome; ABG see Blood gases; Ablatio placentae Acute idiopathic polyneuritis see Guillain-Barre syndrome http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_A-Ag.htm
Extractions: Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z A-Th3 see Antithrombin III A/P repair see Anterior vaginal wall repair A1C see Aarskog syndrome Aase syndrome Aase-Smith syndrome see Aase syndrome AAT deficiency see Alpha-1 antitrypsin deficiency AAT or A1AT see Alpha-1 antitrypsin Abacterial cystitis see Cystitis - noninfectious Abdomen - swollen Abdominal aortic aneurysm Abdominal arteriogram see Mesenteric arteriography Abdominal birth see C-section Abdominal bloating Abdominal cramps see Abdominal pain Abdominal CT scan Abdominal delivery see C-section Abdominal discomfort see Abdominal distress Abdominal distention see Abdomen - swollen Abdominal distress Abdominal exploration Abdominal film ... Abdominal girth Abdominal hernia see Lump in the abdomen Abdominal hysterectomy see Hysterectomy Abdominal mass Abdominal MRI Abdominal pain ... Abdominal pain diagnosis Abdominal pregnancy see Ectopic pregnancy Abdominal rigidity Abdominal sonogram see Abdominal ultrasound Abdominal sounds Abdominal tap Abdominal thrusts see Heimlich maneuver Abdominal ultrasound Abdominal wall biopsy see Abdominal wall fat pad biopsy Abdominal wall defect repair see Gastroschisis repair Abdominal wall defects see Lump in the abdomen Abdominal wall fat pad biopsy Abdominal wall surgery Abdominal x-ray see Abdominal film Abdominoplasty see Abdominal wall surgery Abducens palsy see Cranial mononeuropathy VI Abetalipoproteinemia see Bassen-Kornzweig syndrome ABG see
► Bassen-Kornzweig Syndrome A medical encycopedia article on the topic bassen-kornzweig syndrome. 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).
Dr. Koop - Bassen-Kornzweig Syndrome bassenkornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. It results in http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
► Bassen-Kornzweig Syndrome A medical encycopedia article on the topic bassen-kornzweig syndrome. http://www.umm.edu/ency/article/001666prv.htm
MedlinePlus Medical Encyclopedia Bassen-Kornzweig Syndrome bassenkornzweig syndrome Contents of this page Alternative names. Definition. Causes, incidence, and risk factors. Symptoms. Signs and tests http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Dr. Koop - Bassen-Kornzweig Syndrome bassenkornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut. 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 (
? Bassen-Kornzweig Syndrome A medical encycopedia article on the topic bassen-kornzweig syndrome http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Bassen-Kornzweig Syndrome - General Practice Notebook bassenkornzweig syndrome. Abetalipoproteinaemia is a disorder in the synthesis of serum lipoproteins containing apolipoprotein B, for example chylomicrons, http://www.gpnotebook.co.uk/cache/550502431.htm
ABETALIPOPROTEINAEMIA (BASSEN-KORNZWEIG SYNDROME) Features Listed For ABETALIPOPROTEINAEMIA (bassenkornzweig syndrome) McKusick 200100. Pigmentary retinopathy/chorioretinitis http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
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 (
Extractions: @import url(default.css); Back to Health Library Print This Page Email to a Friend 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 bassenkornzweig syndrome Alternative Names Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency Symptoms http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: @import url(default.css); Back to Health Library Print This Page Email to a Friend 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).
AllRefer Health - Bassen-Kornzweig Syndrome (Abetalipoproteinemia bassenkornzweig syndrome (Abetalipoproteinemia, Acanthocytosis, Apolipoprotein B Deficiency) information center covers causes, prevention, symptoms http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Medical Directory - Information About Bassen-Kornzweig Syndrome Medical Directory Information about bassen-kornzweig syndrome. About Us Privacy Policy FAQs bassen-kornzweig syndrome Bathing trunk nevus http://www.sainetsympa.com/ListingMedicalDirectory-B-1651.htm
Extractions: 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).
Acanthocytosis bassenkornzweig syndrome; Low-Density Beta Lipoprotein Deficiency. Disorder Subdivisions. None. General Discussion. Acanthocytosis is a digestive disorder http://webcenter.health.webmd.netscape.com/hw/skin_and_beauty/nord445.asp
Extractions: 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).
