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BMJ Case Rep ; 13(9)2020 Sep 14.
Article in English | MEDLINE | ID: mdl-32928829

ABSTRACT

Acute necrotising encephalopathy (ANE) is a rare disease that corresponds to a rapidly progressive encephalopathy induced by a viral infection. It is frequently associated with a mutation on the RAN-binding protein 2 (RANBP2) gene-ANE1. We present a case of a 5-year-old boy with a clinical picture of influenza aggravated to an acute encephalopathy picture after the 3rd day. Complementary examinations came back positive for the influenza A virus, and MRI showed aspects compatible with ANE. He was treated accordingly with subsequent improvement of the clinical picture. During ambulatory follow-up, a mutation was detected on the RANBP2 gene and, at the ophthalmological level, bilateral peripheral constriction on the campimetry and a significant reduction of bilateral peripapillary retinal nerve fibre layer was reported. Our case contributes to the enrichment of the neuro-ophthalmological literature and expands the spectrum of sequelae of this rare entity in the Caucasian population.


Subject(s)
Encephalitis, Viral/genetics , Influenza A virus/genetics , Influenza, Human/physiopathology , Child, Preschool , Cough/etiology , Fever/etiology , Genetic Predisposition to Disease , Humans , Influenza A virus/pathogenicity , Influenza, Human/genetics , Magnetic Resonance Imaging/methods , Male , Rhinorrhea/etiology
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