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Genetic causes of infection induced encephalitis.
Quinn, Olivia-Paris; McNaughton, Peter; Pereira, Nolette; Riney, Kate.
Affiliation
  • Quinn OP; Department of Neurosciences, Queensland Children's Hospital, Queensland, Australia; The University of Queensland, Queensland, Australia. Electronic address: Olivia-paris.quinn@health.qld.gov.au.
  • McNaughton P; The University of Queensland, Queensland, Australia; Department of Immunology and Allergy, Queensland Children's Hospital, Queensland, Australia.
  • Pereira N; Department of Radiology, Queensland Children's Hospital, Queensland, Australia.
  • Riney K; Department of Neurosciences, Queensland Children's Hospital, Queensland, Australia; The University of Queensland, Queensland, Australia.
Eur J Paediatr Neurol ; 50: 16-22, 2024 May.
Article in En | MEDLINE | ID: mdl-38564873
ABSTRACT

INTRODUCTION:

Patients with encephalitis following a viral infection are often thought to have a para infectious, inflammatory, or autoimmune cause for their presentation. These diagnoses usually result in treatments with immunosuppressant therapies which can have side effects. However, there is an increasing body of evidence demonstrating that patients can have a direct genetic cause mediating viral infection triggered encephalitis, where inflammation is a secondary response. These patients may benefit not from immunosuppressive therapies, but from protection from infection through dedicated immunisation programs and early antiviral therapies at times of infection.

METHODS:

A small case series of paediatric neurology patients (n = 2) from a single institution with infection induced encephalitis and an underlying genetic cause, is presented. Patients with a confirmed genetic cause of infection induced encephalitis were identified and consented by their treating neurologist for inclusion in this case series. Ethics approval was gained for this case series and review of the surrounding literature.

CONCLUSION:

A case of both DBR1 and NUP214 genetic changes resulting in infection induced encephalitis is presented. This case series raises awareness of this rare group of disorders and provides clues to their identification. Features to prompt clinician consideration of such genetic conditions are also highlighted. Although rare, identification of these patients is important due to implications on treatment, prognosis, and family planning.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nuclear Pore Complex Proteins Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Nuclear Pore Complex Proteins Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Eur J Paediatr Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2024 Type: Article