原血漿銅藍蛋白缺乏症
Also known as ACERULOPLASMINEMIA, Hemosiderosis, Systemic, Due to Aceruloplasminemia, Hypoceruloplasminemia, Hereditary ceruloplasmin deficiency, Systemic hemosiderosis due to aceruloplasminemia, Familial apoceruloplasmin deficiency, Ceruloplasmin Deficiency
Aceruloplasminemia is a rare autosomal recessive disorder in which the liver can not synthesize the protein ceruloplasmin properly, which is needed to transport copper around the blood. Copper deficiency in the brain results in neurological problems that generally appear in adulthood and worsen over time.
Key facts
- Medical condition (new).name
- Aceruloplasminemia
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- File:Iron deposition in globus pallidus.jpg
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- MRI hypointensity (white arrows) in the globus pallidi that indicates the presence of iron deficiencies which would be seen in a diagnosis of Aceruloplasminemia
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- Medical genetics
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- Ceruloplasmin deficiency
via Wikipedia infobox
Research
287 papers- Aceruloplasminemia.1993
- [Aceruloplasminemia, a rare condition not to be overlooked].La Revue de medecine interne · 2020
- Aceruloplasminemia.Current drug targets · 2012
- Aceruloplasminemia.