| Literature DB >> 26407445 |
M-L Frémond1, P Pérot2, E Muth3, G Cros1, M Dumarest2, N Mahlaoui4, D Seilhean5, I Desguerre6, C Hébert3, N Corre-Catelin7, B Neven1, M Lecuit8, S Blanche1, C Picard9, M Eloit10.
Abstract
A boy with X-linked agammaglobulinemia experienced progressive global motor decline, cerebellar syndrome, and epilepsy. All standard polymerase chain reactions for neurotropic viruses were negative on cerebrospinal fluid and brain biopsy. Next-generation sequencing allowed fast identification of a new astrovirus strain (HAstV-VA1/HMO-C-PA), which led to tailor the patient's treatment, with encouraging clinical monitoring over 1 year.Entities:
Keywords: Bruton; agammaglobulinemia; astrovirus; encephalitis
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Year: 2015 PMID： 26407445 DOI： 10.1093/jpids/piv040
Source DB: PubMed Journal: J Pediatric Infect Dis Soc ISSN： 2048-7193 Impact factor: 3.164