Find Expert Doctors on Familial apoceruloplasmin deficiency207 top medical experts on Familial apoceruloplasmin deficiency across 20 countries and 6 U.S. states, including 37 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Familial apoceruloplasmin deficiency: A rare adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- NBIA Disorders Association
2082 Monaco Ct.
El Cajon, CA 92019-4235
Telephone: +1-619-588-2315
Fax: +1-619-588-4093
E-mail: info@NBIAdisorders.org
Website: https://www.nbiadisorders.org/
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- Synonyms: Aceruloplasminemia, Ceruloplasmin deficiency, Hereditary hypoceruloplasminemia, Hypoceruloplasminemia
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