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Globus Pallidus Lesion With Iron Deposition and Dopaminergic Denervation in a Patient With a Pathogenic SLC6A1 Variant: A Case Report.
Leclert, Victoire; Laurencin, Chloe; Ameli, Roxana; Hermier, Marc; Flaus, Anthime; Prange, Stephane; Lesca, Gaetan; Thobois, Stephane.
Afiliação
  • Leclert V; From 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 M
  • Laurencin C; From 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 M
  • Ameli R; From 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 M
  • Hermier M; From 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 M
  • Flaus A; From 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 M
  • Prange S; From 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 M
  • Lesca G; From 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 M
  • Thobois S; From 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 M
Neurol Genet ; 10(2): e200136, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38515990
ABSTRACT

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-ß-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-ß-CIT SPECT were performed.

Results:

MRI of the brain found bilateral pallidal lesions consistent with neurodegeneration with iron accumulation. The I123-FP-ß-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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Neurol Genet Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Neurol Genet Ano de publicação: 2024 Tipo de documento: Article