Bassen Kornzweig Syndrome also known as Abetalipoproteinemia; Acanthocytosis; Apolipoprotein B deficiency is an autosomal recessive condition that more often affects males, but can also affect girls. It is caused by a defect in the microsomal triglyceride transfer protein (MTP) gene. The defect makes the body unable to create lipoproteins (molecules of fat combined with protein). Persons with this condition are unable to properly digest fat and essential vitamins.

A Cure for Bassen Kornzweig Foundation is dedicated to education, research and support for Bassen Kornzweig Syndrome. We are dedicated to the diagnosis, treatment, and cure of Bassen Kornzweig Syndrome. We are dedicated to providing support to families and loved ones of this syndrome. read more

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