Abetalipoproteinemia is a relatively rare genetic and acquired disorder that is characterized by acanthocytic red blood cells, fat malabsorption, spinocerebellar degeneration, and pigmented retinopathy.
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Feb 1, 2018 · Abetalipoproteinemia is an inherited disorder that impairs the normal absorption of fats and certain vitamins from the diet.
Abetalipoproteinemia is a rare inherited disorder affecting fat absorption by the intestine and mobilization by the liver. Inability to absorb fat results in ...
Oct 25, 2018 · Abetalipoproteinemia typically presents in infancy with failure to thrive, diarrhea, vomiting, and malabsorption of fat.
Abetalipoproteinemia
Disorder
Abetalipoproteinemia is a disorder characterized by abnormal absorption of fat and fat-soluble vitamins from food. Wikipedia
Abetalipoproteinemia is a disorder characterized by abnormal absorption of fat and fat-soluble vitamins from food. It is caused by a mutation in microsomal ...
Jul 8, 2008 · Abetalipoproteinemia (ABL, OMIM 200100) is a rare, autosomal recessive disorder, characterized by fat malabsorption, acanthocytosis and ...
Abetalipoproteinemia manifests during the first year of life or in young childhood. It is often associated with growth delay, hepatomegaly with steatosis, ...
Jul 22, 2022 · Abetalipoproteinemia is a rare genetic disorder caused by impaired transport of intestinal and hepatic lipids that typically presents in the ...
Feb 1, 2018 · Abetalipoproteinemia is an inherited disorder that impairs the normal absorption of fats and certain vitamins from the diet.