1. 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

@import url(/medlineplus/images/advanced.css); Skip navigation Medical Encyclopedia Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Bassen-Kornzweig syndrome Contents of this page: Alternative names Definition Causes, incidence, and risk factors Symptoms ... Prevention 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 (

2. 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

3. 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

@import url(/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Medical Encyclopedia Topics beginning with "A-Ag" 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

4. HealthCentral - General Encyclopedia - Bassen-Kornzweig Syndrome bassenkornzweig syndrome. Disease Gallery (Select One) http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

5. ► Bassen-Kornzweig Syndrome A medical encycopedia article on the topic bassen-kornzweig syndrome. http://www.umm.edu/ency/article/001666.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Disease Nutrition Surgery Symptoms Injury ... Encyclopedia (English) Toggle English Spanish Bassen-Kornzweig syndrome 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. 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 (

6. 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

7. ► Bassen-Kornzweig Syndrome A medical encycopedia article on the topic bassen-kornzweig syndrome. http://www.umm.edu/ency/article/001666prv.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Disease Nutrition Surgery Symptoms Injury ... Encyclopedia (English) Toggle English Spanish Bassen-Kornzweig syndrome Overview Symptoms Treatment Prevention Alternative Names: Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency Prevention: High doses of fat soluble vitamins may be able to slow progression of some problems such as degeneration of the retina and decreased vision. Review Date: 10/30/2001 Reviewed By: David G. Brooks, M.D., Ph.D., Division of Medical Genetics, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

8. 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

9. 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

Home Health Reference Bassen-Kornzweig syndrome Jul 29, 2005 Search: Dr.Koop MEDLINE Diseases Symptoms Procedures Natural Medicine ... Drug Library Inside DrKoop News Archive Animations Health Videos Health Tools ... Newsletters Bassen-Kornzweig syndrome Injury Disease Nutrition Poison ... Prevention 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 (

10. ? 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

11. 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

Bassen-Kornzweig syndrome Abetalipoproteinaemia is a disorder in the synthesis of serum lipoproteins containing apolipoprotein B, for example chylomicrons, VLDL and LDL. Click here for more information...

12. 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

13. Bassen-Kornzweig Syndrome Medical Information bassenkornzweig syndrome Information from Drugs.com. http://www.drugs.com/enc/bassen_kornzweig_syndrome.html

Home New Drugs Latest News Drug Interactions ... Forum Drugs.com - prescription drug and medicine information available on over 24,000 approved- medications and pharmaceuticals, including side effects and drug interactions. Log-in Register Advertisement Buy a Link Now Special Offers From our sponsors Categories Diabetes Gastro Center Weight Loss AIDS/HIV ... Sexual Health Advertisement Advanced Search Or click the first letter of a drug name: A B C D ... Z Bassen-Kornzweig syndrome Injury Disease Nutrition Poison ... Z 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 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 (

14. Abetalipoproteinemia (Bassen Kornzweig Syndrome) Abetalipoproteinemia (Bassen Kornzweig Syndrome) abetalipoproteinemia. Abetalipoproteinaemia (bassenkornzweig syndrome) Abetalipoproteinemia http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

15. Bassen-Kornzweig Syndrome - Alegent Health Serving Eastern Nebraska And Southwes bassenkornzweig syndrome - courtesy of Alegent Health serving eastern Nebraska and southwest Iowa - Council Bluffs, Iowa - Corning, Iowa - Missouri Valley, http://www.alegent.com/11234.cfm

@import url(default.css); Back to Health Library Print This Page Email to a Friend 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.

16. 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

17. Bassen-Kornzweig Syndrome - SWMC Serving Vancouver Washington Portland Oregon bassenkornzweig syndrome - Online Medical Encyclopedia courtesy of Southwest Washington Medical Center, a Top 100 Hosptital award winner locacted in http://www.swmedicalcenter.com/117351.cfm

@import url(default.css); Health Information Manager Back to Health Library Print This Page Email to a Friend 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.

18. 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

19. 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

Medical Directory - Information about Bassen-Kornzweig syndrome About Us FAQs Home Home ... Disease . Bassen-Kornzweig syndrome Information about Bassen-Kornzweig syndrome 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). People with this disease are unable to properly digest fat, and have underdeveloped nerves (neuropathy), poor muscle coordination (ataxia

20. 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

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center XML News via RSS Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Health Tools Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map You are in Women, Men, Lifestyle Choose a Topic Overview Aging Alternative Medicine Dental Emotional Wellness Eye Health Fitness Healthy Sexuality Men Women Health Topics Symptoms Medical Tests Medications ... For a Complete Report Acanthocytosis Important It is possible that the main title of the report Acanthocytosis is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms Bassen-Kornzweig Syndrome Low-Density Beta Lipoprotein Deficiency Disorder Subdivisions None General Discussion 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). Resources CLIMB (Children Living with Inherited Metabolic Diseases)

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