Aceruloplasminemia

An adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms.

Also known as: cerebellar ataxia, aceruloplasminemia, hereditary ceruloplasmin deficiency, hypoceruloplasminemia, hereditary, ceruloplasmin deficiency, familial apoceruloplasmin deficiency, hemosiderosis, systemic, due to aceruloplasminemia, hypoceruloplasminemia

46 clinical trials for this condition and its sub-types.