Spinal atrophy-ophthalmoplegia-pyramidal syndrome

Spinal atrophy-ophthalmoplegia-pyramidal syndrome is a rare, bulbospinal muscular atrophy characterized by generalized neonatal hypotonia, progressive pontobulbar and spinal palsy, pyramidal signs, and deafness. External ophthalmoplegia and bilateral mydriasis are typical signs. There have been no further descriptions in the literature since 1994.

Also known as: Hamano-Tsukamoto syndrome, Hamano Tsukamoto syndrome, infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms, spinal atrophy ophthalmoplegia pyramidal syndrome

10 clinical trials for this condition and its sub-types, 0 tagged with Spinal atrophy-ophthalmoplegia-pyramidal syndrome itself.