GJB2 and sensorineural hearing loss disorder: The articles primarily reported the aetiology of SNHL as ‘congenital’ and/or ‘early onset’, with some articles focusing on specific target aetiology such as Usher syndrome Type 1, congenital cytomegalovirus (cCMV), connexin 26 mutations, rubella, and autosomal recessive hereditary nonsyndromic deafness.