Aceruloplasminemia
Synonyms: Hereditary ceruloplasmin deficiency
A rare adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia retinal degeneration diabetes and various neurological symptoms.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Aceruloplasminemia?
Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.
Advocacy Organizations
KIF1A.ORG
KIF1A.ORG is a global community dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder (KAND) and accelerating research to find a cure.
NBIA Disorders Association
In our drive to find a cure for Neurodegeneration with Brain Iron Accumulation, we provide support to families, educate the public, and accelerate research with collaborators from around the world.
Clinical Trials
For a list of clinical trials in this disease area, please click here.