| Literature DB >> 19643689 |
E López-Laso1, M E Mateos-González, J L Pérez-Navero, R Camino-León, P Briones, D E Neilson.
Abstract
Acute necrotizing encephalopathy (ANE) presents in children after common viral infections. Most cases of ANE are non-familial and non-recurrent and have been mainly reported in Asian patients, although ANE affects children worldwide. Recently, missense mutations in the gene encoding the nuclear pore protein Ran Binding Protein 2 (RANBP2) have been found in several families with familial or recurrent cases of ANE. We describe a Spanish family with familial and recurrent ANE without mutations in RANBP2. Mutations in RANBP2 are not the sole susceptibility alleles for familial or recurrent ANE.Entities:
Mesh:
Year: 2009 PMID: 19643689 DOI: 10.1016/j.anpedi.2009.05.020
Source DB: PubMed Journal: An Pediatr (Barc) ISSN: 1695-4033 Impact factor: 1.500