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Case Reports
. 2021 Feb 17;12(2):163-166.
doi: 10.1055/s-0041-1723959. eCollection 2023 Jun.

Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders

Affiliations
Case Reports

Eye of the Tiger: Looking Beyond Neurodegeneration with Brain Iron Accumulation Disorders

Prajnya Ranganath et al. J Pediatr Genet. .

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.

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Conflict of interest statement

Conflict of Interest None declared.

Figures

Fig. 1
Fig. 1
( A ) Close-up of the child's face showing the coarse facial features, mild ocular hypertelorism, and broad nasal bridge and thick lips. ( B ) Lateral radiograph of the lumbosacral spine showing the ovoid vertebrae and the anterior-inferior beaking indicative of dysostosis multiplex. ( C ) T2-weighted axial image of MRI brain showing bilaterally symmetrical hypointensity of both the globi pallidi with a central streak of hyperintensity between the medial and lateral segments of the globi pallidi, resembling the “eye-of-the-tiger” sign (pointed out by the arrow), along with symmetric hyperintensities in bilateral cerebral white matter. ( D ) T1-weighted axial image of MRI brain showing bilaterally symmetrical hyperintensity of globi pallidi, substantia nigra, and subthalamic nuclei (pointed out by the arrow). ( E ) Sanger sequence chromatogram of the proband showing the homozygous c.810del variant in the FUCA1 gene (the position of the single nucleotide deletion is marked with the arrow). ( F ) Sanger sequence chromatogram of the mother showing the heterozygous c.810del variant in the FUCA1 gene (the position of the single nucleotide deletion is marked with the arrow).

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