abetalipoproteinemia Sentence Examples
- Abetalipoproteinemia is an inherited disorder that impairs the body's ability to transport fats and fat-soluble vitamins.
- Individuals with abetalipoproteinemia often exhibit symptoms such as malabsorption, leading to deficiencies in essential nutrients.
- Treatment for abetalipoproteinemia typically involves dietary modifications to manage lipid intake and nutritional supplementation.
- The genetic mutation causing abetalipoproteinemia affects the synthesis of apolipoprotein B, a crucial component of lipoproteins.
- People with abetalipoproteinemia may experience neurological complications due to vitamin E deficiency, such as ataxia.
- The diagnosis of abetalipoproteinemia is confirmed through genetic testing, which identifies mutations in the MTP or APOB genes.
- Infants diagnosed with abetalipoproteinemia may show failure to thrive and developmental delays without proper intervention.
- Management of abetalipoproteinemia requires a lifelong commitment to a specific diet that supports adequate nutrient absorption.
- Researchers continue to explore potential therapies to address the underlying genetic abnormalities associated with abetalipoproteinemia.
- Early detection and intervention are crucial in providing the best possible outcomes for individuals with abetalipoproteinemia.
abetalipoproteinemia Meaning
abetalipoproteinemia (n)
a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally low cholesterol levels
Synonyms & Antonyms of abetalipoproteinemia
No Synonyms and anytonyms found
FAQs About the word abetalipoproteinemia
a rare inherited disorder of fat metabolism; characterized by severe deficiency of beta-lipoproteins and abnormal red blood cells (acanthocytes) and abnormally
No synonyms found.
No antonyms found.
Abetalipoproteinemia is an inherited disorder that impairs the body's ability to transport fats and fat-soluble vitamins.
Individuals with abetalipoproteinemia often exhibit symptoms such as malabsorption, leading to deficiencies in essential nutrients.
Treatment for abetalipoproteinemia typically involves dietary modifications to manage lipid intake and nutritional supplementation.
The genetic mutation causing abetalipoproteinemia affects the synthesis of apolipoprotein B, a crucial component of lipoproteins.
