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NBIANational Business Incubation Association
NBIANeurodegeneration with Brain Iron Accumulation (neurological disorder)
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NBIANational BioEnergy Industries Association (Washington, DC)
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NBIANewfoundland Brain Injury Association (Canada)
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References in periodicals archive ?
Pathogenic mutations in the C19orf12 gene result in a rare autosomal recessive condition, mitochondrial membrane protein-associated neurodegeneration (MPAN), (1) part of the type 4 neurodegeneration with brain iron accumulation (NBIA) group of disorders (MIM#614298).
Brain MRI in neurodegeneration with brain iron accumulation with and without PANK2 mutations.
One protein from this family, alpha-synuclein, is found extensively in neurons and is a major component of pathological inclusions that characterize several neurodegenerative disorders, including Parkinson's disease, dementia with Lewy bodies, neurodegeneration with brain iron accumulation type 1, and multiple system atrophy, which collectively are termed synucleinopathies.
1) The sign is considered as the distinctive radiologic feature of Neurodegeneration with Brain Iron Accumulation (NBIA) type 1, also known as Pantothenate Kinase Associated Neurodegeneration (PKAN).