Advanced genetic testing vital
HSP is commonly misdiagnosed as Cerebral Palsy in children under 3 years old. Whole exome sequencing (WES) identified established or likely HSP mutations in 6 genes in children from 14 families. This highlights the importance of genetic testing for accurate diagnosis, prognosis and management of HSP in affected children.
Spastic diplegia presenting in infancy is common to both cerebral palsy (CP) and hereditary spastic paraplegia (HSP). We report the clinical and genetic features of a cohort of Alberta patients with a diagnosis of HSP, who were initially diagnosed with CP.
Fourteen patients with an initial diagnosis of CP were identified from an Alberta registry of HSP patients via chart review. Whole exome sequencing (WES) was performed to identify genetic causes.
From 90 families in the database, individuals in 29 families had a pediatric presentation of spasticity, with 20 presenting under 3 years of age. Individuals from 14 families had received an initial diagnosis of CP and correct diagnosis was made after neurogenetic assessment due to symptom progression. All had early onset (<3 years) of symptoms. WES identified pathogenic or likely pathogenic mutations in nine cases involving six genes: ATL1, PLP1, PNPLA6, SACS, SPAST, and SYNE1. In five families, WES did not reveal a genetic etiology but progression of symptoms and positive family history suggests HSP is the most likely diagnosis.
In our cohort, 70% of HSP children presenting with spasticity under 3 years had been misdiagnosed with CP. In a young child presenting with spastic diplegia without clear history of prematurity, intrauterine growth restriction, infection or vascular insult, it is important to consider HSP. Accurate diagnosis has implications for prognosis, management, and recurrence risk.
SOURCE: Clin Park Relat Disord. 2021 Nov 3;5:100114. doi: 10.1016/j.prdoa.2021.100114. eCollection 2021. PMID: 34816117
Hereditary spastic paraplegia initially diagnosed as cerebral palsy
Oksana Suchowerskya1, Setareh Ashtianib, Ping-Yee Billie Aub, Scott McLeodc, Mehrdad A.Estiard, ZivGan-Orde, Guy A.Rouleaude
A. University of Alberta, Departments of Medicine (Neurology) and Medical Genetics, Edmonton, Canada
B. Alberta Children’s Hospital, Medical Genetics, Calgary, Canada
C. Alberta Children’s Hospital, Developmental Pediatrics, Calgary, Canada
D. McGill University, Department of Human Genetics, Montreal, Canada
E. McGill University, Department of Neurology and Neurosurgery, Montreal, Canada.