Encyclopedia
Abetalipoproteinemia is an inherited disorder that impairs the normal absorption of fats and certain vitamins from the diet. Many of the signs and symptoms of abetalipoproteinemia result from a severe shortage (deficiency) of fat-soluble vitamins (vitamins A, E, and K). The signs and symptoms of this condition primarily affect the gastrointestinal system, eyes, nervous system, and blood.
- genetic conditions
1. Introduction
The first signs and symptoms of abetalipoproteinemia appear in infancy. They often include failure to gain weight and grow at the expected rate (failure to thrive); diarrhea; and fatty, foul-smelling stools (steatorrhea).
As an individual with this condition ages, additional signs and symptoms include disturbances in nerve function that may lead to poor muscle coordination and difficulty with balance and movement (ataxia). They can also experience a loss of certain reflexes, impaired speech (dysarthria), tremors or other involuntary movements (motor tics), a loss of sensation in the extremities (peripheral neuropathy), or muscle weakness. The muscle problems can disrupt skeletal development, leading to an abnormally curved lower back (lordosis), a rounded upper back that also curves to the side (kyphoscoliosis), high-arched feet (pes cavus), or an inward- and upward-turning foot (clubfoot).
Individuals with this condition may also develop an eye disorder called retinitis pigmentosa, in which breakdown of the light-sensitive layer (retina) at the back of the eye can cause vision loss. In individuals with abetalipoproteinemia, the retinitis pigmentosa can result in complete vision loss. People with abetalipoproteinemia may also have other eye problems, including involuntary eye movements (nystagmus), eyes that do not look in the same direction (strabismus), and weakness of the external muscles of the eye (ophthalmoplegia).
Individuals with abetalipoproteinemia usually have a low number of red blood cells (anemia) with abnormally star-shaped red blood cells (acanthocytosis) and have difficulty forming blood clots, which can cause abnormal bleeding. In some cases, a condition called fatty liver develops, which can cause liver damage.
2. Frequency
Abetalipoproteinemia is a rare disorder. More than 100 cases have been described worldwide.
3. Causes
Abetalipoproteinemia is caused by mutations in the MTTP gene, which provides instructions for making a protein called microsomal triglyceride transfer protein. This protein is essential for creating molecules called beta-lipoproteins in the liver and intestine. Beta-lipoproteins transport fats, cholesterol, and fat-soluble vitamins from the intestine to the bloodstream so these nutrients can be taken up by tissues throughout the body. Sufficient levels of fats, cholesterol, and vitamins are necessary for normal growth, development, and maintenance of the body's cells and tissues.
Most MTTP gene mutations lead to the production of microsomal triglyceride transfer protein with reduced or absent function and unable to help in the formation of beta-lipoproteins. A lack of beta-lipoproteins causes severely reduced absorption (malabsorption) of dietary fats and fat-soluble vitamins from the digestive tract into the bloodstream. These nutritional deficiencies lead to health problems in people with abetalipoproteinemia.
4. Inheritance
This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
5. Other Names for This Condition
-
abetalipoproteinaemia
-
abetalipoproteinemia neuropathy
-
ABL
-
acanthocytosis
-
apolipoprotein B deficiency
-
Bassen-Kornzweig disease
-
Bassen-Kornzweig syndrome
-
betalipoprotein deficiency disease
-
congenital betalipoprotein deficiency syndrome
-
microsomal triglyceride transfer protein deficiency disease
-
MTP deficiency
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/abetalipoproteinemia
References
- Hooper AJ, van Bockxmeer FM, Burnett JR. Monogenic hypocholesterolaemic lipid disorders and apolipoprotein B metabolism. Crit Rev Clin Lab Sci.2005;42(5-6):515-45. Review.
- Lee J, Hegele RA. Abetalipoproteinemia and homozygous hypobetalipoproteinemia:a framework for diagnosis and management. J Inherit Metab Dis. 2014May;37(3):333-9. doi: 10.1007/s10545-013-9665-4.
- Magnolo L, Najah M, Fancello T, Di Leo E, Pinotti E, Brini I, Gueddiche NM,Calandra S, Slimene NM, Tarugi P. Novel mutations in SAR1B and MTTP genes inTunisian children with chylomicron retention disease and abetalipoproteinemia.Gene. 2013 Jan 1;512(1):28-34. doi: 10.1016/j.gene.2012.09.117.
- Welty FK. Hypobetalipoproteinemia and abetalipoproteinemia. Curr Opin Lipidol.2014 Jun;25(3):161-8. doi: 10.1097/MOL.0000000000000072. Review.
- Zamel R, Khan R, Pollex RL, Hegele RA. Abetalipoproteinemia: two case reports and literature review. Orphanet J Rare Dis. 2008 Jul 8;3:19. doi:10.1186/1750-1172-3-19. Review.
