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Mitochondrial membrane protein associated neurodegeneration: A novel variant of neurodegeneration with brain iron accumulation.
Mov. Disord. 28, 224-227 (2013)
Background Recently, mutations in an open-reading frame on chromosome 19 (C19orf12) were identified as a novel genetic factor in neurodegeneration with brain iron accumulation (NBIA). Because of the mitochondrial localization of the derived protein, this variant is referred to as mitochondrial membrane protein-associated neurodegeneration with brain iron accumulation (MPAN). Methods/Results We describe the clinical phenotype and MRI of 3 newly identified individuals with MPAN due to either previously reported or novel homozygous or compound heterozygous genetic alterations in C19orf12. Conclusions MPAN is characterized by a juvenile-onset, slowly progressive phenotype with predominant lower limb spasticity, generalized dystonia, and cognitive impairment. Typical additional features include axonal motor neuropathy and atrophy of the optic nerve. MRI showed iron deposition in the globus pallidus and substantia nigra without the eye-of-the-tiger sign, which is typical for PKAN, the most frequent form of NBIA.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Neurodegeneration With Brain Iron Accumulation (nbia) ; Genetics ; Mri ; Mitochondrial Membrane Protein-associated Neurodegeneration (mpan) ; C19orf12; Hallervorden-spatz-syndrome ; Dystonia ; Pank2
ISSN (print) / ISBN 0885-3185
Journal Movement Disorders
Quellenangaben Volume: 28, Issue: 2, Pages: 224-227
Reviewing status Peer reviewed
Institute(s) Institute of Human Genetics (IHG)