Abetalipoproteinemia
Abetalipoproteinemia is a rare inherited disorder that impairs the normal absorption of fats and fat-soluble vitamins (A, E, and K) from the diet, leading to a range of signs and symptoms primarily affecting the eyes, nervous system, and blood, often appearing in infancy.
Overview
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 eyes, nervous system, and blood.
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
- 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)
- Loss of certain reflexes
- Impaired speech (dysarthria)
- Tremors or other involuntary movements (motor tics)
- Loss of sensation in the extremities (peripheral neuropathy)
- Muscle weakness
The muscle problems can disrupt skeletal development, leading to:
- An abnormally curved lower back
- A rounded upper back that also curves to the side
- High-arched feet
- An inward- and upward-turning foot
Individuals with this condition may also develop an eye disorder called retinitis pigmentosa, in which breakdown of the light-sensitive layer 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)
- Weakness of the external muscles of the eye (ophthalmoplegia)
Individuals with abetalipoproteinemia usually have a low number of red blood cells 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.
Frequency
Abetalipoproteinemia is a rare disorder. More than 100 cases have been described worldwide.
Causes & Risk Factors
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 and . Beta-lipoproteins 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 into the bloodstream. These nutritional deficiencies lead to health problems in people with abetalipoproteinemia.
Genes Associated with Abetalipoproteinemia
- MTTP
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.
Other Names
- 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