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Abetalipoproteinemia

Also Known As: Abetalipoproteinemia neuropathy

Condition / disease reference page from the Everyone Healthy database.

Connected health information

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Condition overview

Attributes

Ageis Child
Causeis Genetic: autosomal Recessive
Commonalityis rare
Incidenceis approximately 1 in 70,000,000 people

Linked signs and symptoms

11

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Linked drugs / medications

0

No linked drugs are listed yet.

Treatments, therapies and supportive options

4

Grouped by treatment type. These are educational database links, not personal treatment recommendations. Evidence labels are shown only where stored in the EH database.

Linked diagnostic tests and investigations

7

These are pulled from both EH diagnostic-test link tables, including the older large test-link table.

Biological and test markers

3

This visual map uses existing EH database links to show biological agents and lab markers reported as increased, decreased, or associated with this condition. These are educational relationships only; test results must be interpreted by a qualified clinician because ranges vary by lab, method, age, sex and clinical context.

Introduction / full article

Abetalipoproteinemia

ID 1

Abetalipoproteinemia

Vitamin E Supplement High Dosage [1, 2 ]

REcommendation: Strongly in favour 

Level of Evidence:  Moderate level of evidence

Abetalipoproteinemia (also known as Bassen-Kornzweig syndrome) is a recessive disorder that impedes the digestion of dietary fats, cholesterol and fat-soluble vitamins. Patients affected by the condition are unable to produce certain lipoproteins and fats, leading to deficiencies of the fat-soluble vitamins A, D, E and K.

 

Causes

This disorder is linked to a mutation in the microsomal triglyceride transfer protein (MTTP) gene, which provides instructions for the production of a protein imperative to the creation of lipoproteins. These lipoproteins are, in turn, essential for the absorption of fats, cholesterol and fat-soluble vitamins from food, and the transport of these nutrients to the bloodstream.

 

Symptoms and diagnosis

The symptoms of abetalipoproteinemia appear in early childhood, and will indicate that the body is not making or absorbing the nutrients that it requires. These include:

·         Failure to gain weight and grow in infancy;

·         Pale, foul-smelling, fatty stools; and

·         Presence of fat and/or blood in stools.

Other symptoms will result from a severe vitamin deficiency, such as:

·         Poor muscle coordination;

·         Degeneration of the retina, leading to near-blindness;

·         Developmental delay or mental retardation; and

·         Scoliosis (curvature) of the spine.

Abetalipoproteinemia can be clinically diagnosed by the analysis and subsequent detection of fat in foul-smelling stools. Similarly, a deficiency of the affected nutrients in the bloodstream can also be used as an indicator.

 

Treatment

Treatment for abetalipoproteinemia typically involves a controlled diet including high levels of vitamin E. This helps the body to produce and restore other missing nutrients, such lipoproteins.

Conditions arising from vitamin deficiency, for example muscle weakness and poor coordination, can be remedied with physiotherapy and/or occupational therapy.

References. 

1. https://rarediseases.org/rare-diseases/abetalipoproteinemia/

2. http://emedicine.medscape.com/article/121975-treatment