Ontology highlight
ABSTRACT:
SUBMITTER: Sumalde AAM
PROVIDER: S-EPMC10137884 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature
Sumalde Angelo Augusto M AAM Scholes Melissa A MA Kalmanson Olivia A OA Terhune Elizabeth A EA Frejo Lidia L Wethey Cambria I CI Roman-Naranjo Pablo P Carry Patrick M PM Gubbels Samuel P SP Lopez-Escamez Jose A JA Hadley-Miller Nancy N Santos-Cortez Regie Lyn P RLP
Genes 20230330 4
Vertigo due to vestibular dysfunction is rare in children. The elucidation of its etiology will improve clinical management and the quality of life of patients. Genes for vestibular dysfunction were previously identified in patients with both hearing loss and vertigo. This study aimed to identify rare, coding variants in children with peripheral vertigo but no hearing loss, and in patients with potentially overlapping phenotypes, namely, Meniere's disease or idiopathic scoliosis. Rare variants w ...[more]