Definition of abetalipoproteinaemia in English:

abetalipoproteinaemia

(also abetalipoproteinemia, a-β-lipoproteinaemia)

noun eɪˌbiːtəlʌɪpə(ʊ)ˌprəʊtiːˈniːmɪəeɪˌbiːtəlɪpə(ʊ)ˌprəʊtiːˈniːmɪə

Medicine

A rare inherited (autosomal recessive) disorder characterized by absence of certain types of lipoprotein from the blood, malabsorption of fat and fat-soluble vitamins, and acanthocytosis, often with retinal and neuromuscular abnormalities.

Origin

1960s. From a- + beta + lipoprotein + -aemia.

Definition of abetalipoproteinaemia in US English:

abetalipoproteinaemia

(also abetalipoproteinemia, a-β-lipoproteinaemia)

noun

Medicine

A rare inherited (autosomal recessive) disorder characterized by absence of certain types of lipoprotein from the blood, malabsorption of fat and fat-soluble vitamins, and acanthocytosis, often with retinal and neuromuscular abnormalities.

Origin

1960s. From a- + beta + lipoprotein + -aemia.

单词	abetalipoproteinaemia
释义	Definition of abetalipoproteinaemia in English: abetalipoproteinaemia (also abetalipoproteinemia, a-β-lipoproteinaemia) noun eɪˌbiːtəlʌɪpə(ʊ)ˌprəʊtiːˈniːmɪəeɪˌbiːtəlɪpə(ʊ)ˌprəʊtiːˈniːmɪə Medicine A rare inherited (autosomal recessive) disorder characterized by absence of certain types of lipoprotein from the blood, malabsorption of fat and fat-soluble vitamins, and acanthocytosis, often with retinal and neuromuscular abnormalities. Origin 1960s. From a- + beta + lipoprotein + -aemia. Definition of abetalipoproteinaemia in US English: abetalipoproteinaemia (also abetalipoproteinemia, a-β-lipoproteinaemia) noun Medicine A rare inherited (autosomal recessive) disorder characterized by absence of certain types of lipoprotein from the blood, malabsorption of fat and fat-soluble vitamins, and acanthocytosis, often with retinal and neuromuscular abnormalities. Origin 1960s. From a- + beta + lipoprotein + -aemia.
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