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Globus Pallidus Lesion With Iron Deposition and Dopaminergic Denervation in a Patient With a Pathogenic SLC6A1
Victoire Leclert1, Chloe Laurencin1, Roxana Ameli1
1From the Department of Neurology C (V.L., C.L., S.P., S.T.), Expert Parkinson Center NS-PARK/FCRIN, Hospices Civils de Lyon, Pierre Wertheimer Neurological Hospital, Bron; Lyon Neuroscience Research Center (C.L., A.F.), UMR5292, INSERM U1028/CNRS; Department of Neuroradiology (R.A., M.H.); Nuclear Medicine Department (A.F.), Hospices Civils de Lyon, Pierre Wertheimer Neurological Hospital; Marc Jeannerod Cognitive Neuroscience Institute (S.P., S.T.), CNRS, UMR 5229, Bron; Faculté de Médecine et Maïeutique Lyon Sud Charles-Mérieux (S.P., G.L., S.T.), Université de Lyon, Université Claude-Bernard Lyon I; Department of Genetics (G.L.), Hospices Civils de Lyon, Mother Child Hospital, Bron; and Physiopathology and Genetics of Neurons and Muscles (G.L.), UMR5261, U1315, Institut NeuroMyoGène, Lyon, France.
Objectives:
SLC6A1-related disorders encompass heterogeneous neuropsychiatric manifestations through GABAergic dysregulation, without any specific abnormalities on brain MRI, nor evidence of dopaminergic cell loss on I123-FP-β-CIT SPECT. We report here a case of globus pallidus lesions and dopaminergic denervation in a patient with a pathogenic SLC6A1 variant.
Methods:
A 26-year-old female patient with intellectual disability, behavioral, and psychiatric disorders treated by neuroleptics for many years developed a parkinsonian syndrome associated with mild hand dystonia and chorea. A 3T brain MRI and I123-FP-β-CIT SPECT were performed.
Results:
MRI of the brain found bilateral pallidal lesions consistent with neurodegeneration with iron accumulation. The I123-FP-β-CIT SPECT showed bilateral striatal presynaptic dopaminergic denervation. Whole-genome sequencing revealed a pathogenic SLC6A1 de novo variant. No additional variant was found in any of the genes responsible for Neurodegeneration with Brain Iron Accumulation (NBIA).
Discussion:
This is a description of dopaminergic denervation and globus pallidus lesions with iron accumulation related to a SLC6A1 pathogenic variant. These findings expand the phenotype of SLC6A1-related disorder and suggest that it could be considered as a differential diagnosis of NBIA.
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