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         Bassen-kornzweig Syndrome:     more detail
  1. Bassen-Kornzweig syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005

1. 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
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Bassen-Kornzweig syndrome
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 (

2. 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

3. 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
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Disease - 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 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).
People with this disease are unable to properly digest fat, and have underdeveloped nerves (neuropathy), poor muscle coordination ( ataxia ), and other nerve disorders.

4. Bassen-Kornzweig Syndrome
Symptoms. Treatment. Prevention. bassenkornzweig syndrome. Alternative Names
http://www.drkoop.com/ency/article/001666prv.htm
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Bassen-Kornzweig syndrome
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: 8/6/2003
Reviewed By: Douglas R. Stewart, M.D., Division of Medical Genetics, Hospital of the University of Pennsylvania, Philadelphia, PA. Review provided by VeriMed Healthcare Network.
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5. 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
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6. 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.
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Medical Encyclopedia: Bassen-Kornzweig syndrome
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).
People with this disease are unable to properly digest fat, and have underdeveloped nerves (neuropathy), poor muscle coordination (ataxia), and other nerve disorders.

7. 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
Bassen-Kornzweig syndrome
A Medical Encyclopedia Article provided by the University of Maryland Medical System A resource with information on over 4000 medical topics including: Bassen-Kornzweig syndrome
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8. HealthCentral - General Encyclopedia - Bassen-Kornzweig Syndrome
General Health Encyclopedia, bassenkornzweig syndrome.
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9. HealthCentral - Pediatrics Encyclopedia - Bassen-Kornzweig Syndrome
Pediatric Health Encyclopedia, bassenkornzweig syndrome.
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10. 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
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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 (

11. AllRefer Health - Bassen-Kornzweig Syndrome (Abetalipoproteinemia, Acanthocytosi
bassenkornzweig syndrome. bassen-kornzweig syndrome is a rare, inherited disease characterized by the inability to fully absorb dietary fats through the gut.
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Alternate 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. 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 (

12. AllRefer Health - Bassen-Kornzweig Syndrome Complications (Abetalipoproteinemia,
You are here AllRefer.com Health Diseases Conditions bassenkornzweig syndrome Complications of bassen-kornzweig syndrome. bassen-kornzweig syndrome.
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You are here : AllRefer.com Health Bassen-Kornzweig Syndrome : Complications of Bassen-Kornzweig Syndrome
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Alternate Names : Abetalipoproteinemia, Acanthocytosis, Apolipoprotein B Deficiency Complications
  • Blindness Mental deterioration Loss of function of peripheral nerves, ataxia

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Complications Calling Your Health Care Provider Topics that might be of interest to you Failure to Thrive CBC LDL Triglyceride Level ... VLDL Other Topics Blindness Cholesterol Fat Movement - Uncoordinated ... Vitamin K Review Date : 8/6/2003 Reviewed By : Douglas R. Stewart, M.D., Division of Medical Genetics, Hospital of the University of Pennsylvania, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

13. ► 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
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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 ( ataxia ), and other nerve disorders.

14. Disease - Bassen-Kornzweig Syndrome - Hartford, Connecticut , Saint Francis Care
Adam Article Manager, Back. Back to main Health Information page Disease bassen-kornzweig syndrome. Definition Bassen-Kornzweig
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Disease - 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 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).
People with this disease are unable to properly digest fat, and have underdeveloped nerves (neuropathy), poor muscle coordination (

15. 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

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Bassen-Kornzweig syndrome
Causes and Risks:
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).
People with this disease are unable to properly digest fat and have underdeveloped nerves (neuropathy), poor muscle coordination ( ataxia ), and other nerve disorders.
Symptoms:

Signs and Tests:
  • CBC that shows abnormally shaped red blood cells (thorny appearance) cholesterol studies, including

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

17. 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

18. Abetalipoproteinemia (Bassen Kornzweig Syndrome)
abetalipoproteinemia. Abetalipoproteinaemia (bassenkornzweig syndrome) Abetalipoproteinemia. abetalipoproteinemia. ABETALIPOPROTEINEMIA. Abetalipoproteinemia. bassen-kornzweig syndrome. HOME. ( )
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19. A-Beta-Lipoproteinemia,Bassen-Kornzweig Syndrome,Betalipoprotein Deficiency,A-Be
ABeta-Lipoproteinemia also known as bassen-kornzweig syndrome Betalipoprotein Deficiency Acanthocytosis bassen-kornzweig syndrome. Available online.
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).

20. Definitions Of Genetic Disorders-B.
htm Barth syndrome mitoch.htm Bartter s Syndrome bartters.htm Basal Cell Nevus Syndrome nbcc.htm Basedow Disease graves.htm bassenkornzweig syndrome abl.htm
http://www.icomm.ca/geneinfo/def-b.htm
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DISORDERS GLOSSARY
Definitions of Genetic Disorders beginning with the letter B Click on the link next to the disorder to view its definition.
B-K Mole Syndrome dns.htm
Babinski-Froelich Syndrome froelich.htm
BADS albinism.htm
Baillarger's Syndrome freys.htm
Balkan Disease santavori.htm
Baller-Gerold Syndrome baller.htm Ballooning Mitral Valve mvp.htm Balo Disease Concentric Sclerosis balo.htm Baltic Myoclonus Epilepsy mpfe.htm Bannayan-Zonana syndrome (BZS) brrs.htm Bannayan-Riley-Ruvalcaba syndrome brrs.htm Banti's Disease banti.htm Bardet-Biedl Syndrome bardet.htm Bare Lymphocyte Syndrome scid.htm Barlow's syndrome mvp.htm Barraquer-Simons Disease lipodyst.htm Barrett Esophagus barrett.htm Barrett Ulcer barrett.htm

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