Brain magnetic resonance imaging findings and auditory brainstem response in a child with spastic paraplegia 2 due to a PLP1 splice site mutation

• DOI: 10.1016/j.braindev.2014.03.001
• Publication Date: 2014-03-28T20:42:21Z
• Authors: Kazuo Kubota; Yoshiaki Saito; Chihiro Ohba; Hirotomo Saitsu; Tetsuhiro Fukuyama; Akihiko Ishiyama; Takashi Saito; Hirofumi Komaki; Eiji Nakagawa; Kenji Sugai; Masayuki Sasaki; Naomichi Matsumoto
• Keywords: Dysarthria; Paraplegia; Hereditary Spastic Paraplegia; Auditory brainstem response; Splice site mutation

A boy with spastic paraplegia type 2 (SPG2) due to a novel splice site mutation of PLP1 presented with progressive spasticity of lower limbs, which was first observed during late infancy, when he gained the ability to walk with support. His speech was slow and he had dysarthria. The patient showed mildly delayed intellectual development. Subtotal dysmyelination in the central nervous system was revealed, which was especially prominent in structures known to be myelinated during earlier period, whereas structures that are myelinated later were better myelinated. These findings on the brain magnetic resonance imaging were unusual for subjects with PLP1 mutations. Peaks I and II of the auditory brainstem response (ABR) were normally provoked, but peaks III-V were not clearly demarcated, similarly to the findings in Pelizaeus-Merzbacher disease. These findings of brain MRI and ABR may be characteristic for a subtype of SPG2 patients.