| Literature DB >> 24685771 |
Kazuo Kubota1, Yoshiaki Saito2, Chihiro Ohba3, Hirotomo Saitsu3, Tetsuhiro Fukuyama4, Akihiko Ishiyama1, Takashi Saito1, Hirofumi Komaki1, Eiji Nakagawa1, Kenji Sugai1, Masayuki Sasaki1, Naomichi Matsumoto3.
Abstract
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.Entities:
Keywords: Auditory brainstem response; Dysmyelination; PLP1; Pelizaeus–Merzbacher disease; Spastic paraplegia 2
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Year: 2014 PMID: 24685771 DOI: 10.1016/j.braindev.2014.03.001
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961