Abetalipoproteinemia, or Bassen-Kornzweig syndrome, is a rare autosomal
recessive disorder that interferes with the normal absorption of fat and fat-soluble
Abetalipoproteinemia is an inherited disorder that affects the absorption of dietary
fats, cholesterol, and fat-soluble vitamins. People affected by this disorder are ...
Abetalipoproteinemia is a rare inherited disorder affecting fat metabolism.
Abnormalities in fat metabolism result in malabsorption of dietary fat and various
Jul 8, 2008 ... Abetalipoproteinemia (ABL, OMIM 200100) is a rare, autosomal recessive
disorder, characterized by fat malabsorption, acanthocytosis and ...
Feb 3, 2016 ... Abetalipoproteinemia (ABL) is an inherited condition that prevents the body from
completely absorbing certain dietary fats.
Aug 1, 2015 ... Alternative Names. Expand Section. Abetalipoproteinemia; Acanthocytosis;
Apolipoprotein B deficiency. References. Expand Section.
A number sign (#) is used with this entry because abetalipoproteinemia is caused
by homozygous or compound heterozygous mutation in the MTP gene ...
Oct 24, 2012 ... Important It is possible that the main title of the report Abetalipoproteinemia is not
the name you expected. Please check the synonyms listing to ...
Dec 16, 2014 ... Abetalipoproteinemia (ABL) and familial hypobetalipoproteinemia (FHBL) are
relatively uncommon inherited disorders of lipoprotein ...
Abetalipoproteinemia/ homozygous familial hypobetalipoproteinemia (ABL/
HoFHBL) is a severe form of familial hypobetalipoproteinemia (see this term) ...