Search on: BASSEN-KORNZWEIG SYNDROME 
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Descriptor English:   Abetalipoproteinemia 
Descriptor Spanish:   Abetalipoproteinemia 
Descriptor Portuguese:   Abetalipoproteinemia 
Synonyms English:   Bassen-Kornzweig Syndrome
Microsomal Triglyceride Transfer Protein Deficiency  
Tree Number:   C16.320.565.398.500.440.500
C18.452.584.500.875.440.500
C18.452.648.398.500.440.500
Definition English:   An autosomal recessive disorder of lipid metabolism. It is caused by mutation of the microsomal triglyceride transfer protein that catalyzes the transport of lipids (TRIGLYCERIDES; CHOLESTEROL ESTERS; PHOSPHOLIPIDS) and is required in the secretion of BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include defective intestinal lipid absorption, very low serum cholesterol level, and near absent LDL. 
History Note English:   1966(1964) 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
urine ultrasonography
veterinary virology
Record Number:   12 
Unique Identifier:   D000012 

Occurrence in VHL:
 

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