What is another word for Apolipoprotein B Deficiency Disease?
Pronunciation: [ˈapəlˌɪpəpɹˌə͡ʊtiːn bˈiː dɪfˈɪʃənsi dɪzˈiːz] (IPA) 
Apolipoprotein B Deficiency Disease, also known as familial hypobetalipoproteinemia, is a rare genetic disorder characterized by a deficiency of apolipoprotein B. This condition affects the normal transportation and metabolism of lipoproteins, resulting in low levels of cholesterol and triglycerides in the blood. There are several synonyms for Apolipoprotein B Deficiency Disease, including familial hypobetalipoproteinemia, APOB deficiency, and abetalipoproteinemia. These terms are often used interchangeably to describe the same condition. Apolipoprotein B Deficiency Disease primarily affects the liver and intestines, leading to various health complications and symptoms such as fat malabsorption, vitamin deficiencies, and neurological issues. Early diagnosis and appropriate management are crucial in addressing the challenges associated with this disorder.
