| Literature DB >> 29421991 |
Meredith K Gillespie1, Peter Humphreys1,2, Hugh J McMillan1,2, Kym M Boycott1,3.
Abstract
Hereditary spastic paraplegia is a phenotypically and genetically heterogeneous group of neurodegenerative disorders characterized by lower extremity weakness and spasticity. Spastic paraplegia 4 (SPG4), caused by heterozygous mutations in the gene SPAST, typically causes a late-onset, uncomplicated form of hereditary spastic paraplegia in affected individuals. Additional clinical features in SPG4 have been reported on occasion, but no genotype-phenotype correlation has been established. Through targeted clinical testing, we identified 2 unrelated female patients with the same de novo p.Arg499His mutation in SPAST. Both patients presented with early-onset spasticity resulting in delayed motor milestones, which led to a diagnosis of cerebral palsy in one child and tethered cord in the other. Review of the literature identified several patients with mutations at amino acid 499 and early-onset symptoms associated with a risk of cognitive impairment. Early and accurate diagnosis of children with early-onset spasticity is important for informed prognosis and genetic counselling.Entities:
Keywords: SPAST; cerebral palsy; cognitive impairment; early-onset spasticity; next-generation sequencing
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Year: 2018 PMID: 29421991 DOI: 10.1177/0883073818756680
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987