Retinitis pigmentosa-deafness syndrome

An Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has material basis in mutation in the MTTS2 gene in the mitochondrial genome.

Also known as: retinitis pigmentosa-deafness syndrome, RP21, formerly, RP8, formerly, retinitis pigmentosa 21, retinitis pigmentosa 21, formerly, retinitis pigmentosa 8, retinitis pigmentosa 8, formerly

0 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa-deafness syndrome itself.