| Literature DB >> 29287866 |
Stéphanie Paquay1, Elsa Wiame2, Naima Deggouj3, Antonella Boschi4, Romolo Daniele De Siati3, Yves Sznajer5, Marie-Cécile Nassogne6.
Abstract
CAPOS syndrome (cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss) is a rare neurological disorder, recently associated with the c.2452G > A hotspot mutation in the ATP1A3 gene, with sensorineural hearing loss as a prominent feature. We herein report on a girl who has experienced hearing loss for three years following an initial encephalitic episode when aged 15 months old. CAPOS was diagnosed only when she was six years old by targeted testing whilst she displayed optic atrophy, cerebellar signs and areflexia. CAPOS syndrome should be considered in the differential diagnosis of acquired childhood deafness, prompting clinicians to search for associated neurological features.Entities:
Keywords: Areflexia; Ataxia; Auditory neuropathy; CAPOS; Hearing loss; Optic atrophy
Mesh:
Substances:
Year: 2017 PMID: 29287866 DOI: 10.1016/j.ijporl.2017.11.022
Source DB: PubMed Journal: Int J Pediatr Otorhinolaryngol ISSN: 0165-5876 Impact factor: 1.675