Ataxia due to abetalipoproteinemia (Q41024): Difference between revisions
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13 August 2026
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Latest revision as of 07:04, 13 August 2026
Ataxia in the setting of abetalipoproteinemia, a rare autosomal recessive disorder caused by a mutation of the MTP gene coding for microsomal triglyceride transfer protein which impairs the ability to produce very low density lipoprotein. All patients have fat malabsorption, acanthocytosis, hypocholesterolemia, and absent apolipoprotein B.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8A03.13 |
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| English | Ataxia due to abetalipoproteinemia |
Ataxia in the setting of abetalipoproteinemia, a rare autosomal recessive disorder caused by a mutation of the MTP gene coding for microsomal triglyceride transfer protein which impairs the ability to produce very low density lipoprotein. All patients have fat malabsorption, acanthocytosis, hypocholesterolemia, and absent apolipoprotein B. |
Statements
CID11:8A03.13
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dki-india-8A03.13
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Concluído
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13 August 2026
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