Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders
- PMID: 37090832
- PMCID: PMC10118706
- DOI: 10.1055/s-0041-1723959
Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders
Abstract
The "eye-of-the-tiger" sign in brain magnetic resonance imaging (MRI) is typically associated with neurodegeneration with brain iron accumulation disorders, especially pantothenate kinase-associated neurodegeneration. However, very similar neuroimaging findings may be seen in other neurodegenerative disorders involving the basal ganglia. We report here a patient with fucosidosis who had MRI brain findings closely resembling the "eye-of-the-tiger" sign.
Keywords: eye-of-the-tiger sign; fucosidosis; neurodegeneration with brain iron accumulation.
Thieme. All rights reserved.
Conflict of interest statement
Conflict of Interest None declared.
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References
-
- ACMG Laboratory Quality Assurance Committee . Richards S, Aziz N, Bale S. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med. 2015;17(05):405–424. - PMC - PubMed
-
- George H T. 8th ed. New York: McGraw-Hill; 2001. Disorders of glycoprotein degradation: α-mannosidosis, β-mannosidosis, α-fucosidosis and sialidosis; pp. 3507–3533.
-
- Sheth J, Mistri M, Bhavsar R. Lysosomal storage disorders in Indian children with Neuroregression attending a genetic center. Indian Pediatr. 2015;52(12):1029–1033. - PubMed
-
- Wali G, Wali G M, Sue C M, Kumar K R. A novel homozygous mutation in the FUCA1 gene highlighting fucosidosis as a cause of dystonia: case report and literature review. Neuropediatrics. 2019;50(04):248–252. - PubMed
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