Two neurologic facets of CTLA4-related haploinsufficiency.
Journal
Neurology(R) neuroimmunology & neuroinflammation
ISSN: 2332-7812
Titre abrégé: Neurol Neuroimmunol Neuroinflamm
Pays: United States
ID NLM: 101636388
Informations de publication
Date de publication:
07 2020
07 2020
Historique:
received:
26
03
2020
accepted:
15
04
2020
entrez:
6
6
2020
pubmed:
6
6
2020
medline:
14
9
2021
Statut:
epublish
Résumé
To describe the clinical and radiologic neurologic characteristics of patients with cytotoxic T-lymphocyte antigen-4 ( Three patients from 2 families had neurologic manifestations in the context of A 16-year-old boy with a previous diagnosis of combined immunodeficiency presented with severe recurrent episodes of headaches, motor deficit, and seizures associated with waxing and waning gadolinium-enhancing FLAIR cortical/juxtacortical hyperintensities. His sister, who also had combined immunodeficiency, had a brain MRI when she was aged 13 years due to recent headaches and transient right hemianopsia. It revealed a gadolinium-enhancing left occipital white matter hyperintensity. Another 49-year-old woman had progressive visual loss and cerebellar ataxia in the context of recurrent pulmonary infections. All 3 patients were found to have inherited These cases suggest that in addition to the variable clinical penetrance and wide spectrum of
Identifiants
pubmed: 32499327
pii: 7/4/e751
doi: 10.1212/NXI.0000000000000751
pmc: PMC7286662
pii:
doi:
Substances chimiques
CTLA-4 Antigen
0
CTLA4 protein, human
0
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
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