Rydning SL1,2, Dudesek A3,4, Rimmele F3,4, Funke C5, Krüger S5, Biskup S5,6, Vigeland MD7, Hjorthaug HS7, Sejersted Y7, Tallaksen C1,2, Selmer KK1,7, Kamm C3.
Background and Purpose:
Hereditary spastic paraplegias (HSP) are clinically and genetically heterogenous monogenic disorders. To date, nearly 70 genes are known to be causative. The aim of this project was to identify the genetic cause of autosomal dominantly inherited pure HSP in two large, unrelated non-consanguineous families.
The two families were characterized clinically and selected members underwent whole exome sequencing. Potentially disease-causing variants were confirmed by Sanger sequencing and their functional consequences on protein function predicted by bioinformatic prediction tools.
The patients presented with pure spastic paraplegia with age of onset between 9 and 46 years. In both families, a novel heterozygous missense variant in ERLIN2, c.386G>C; p.Ser129Thr, was the only potentially pathogenic variant identified that segregated with the disease.
Biallelic variants in ERLIN2 are known to cause recessive HSP type SPG18. Here, we describe the first two families with an autosomal dominant, pure form of HSP caused by a novel ERLIN2 heterozygous missense variant. These findings expand the mutational and inheritance spectrum of SPG18. ERLIN2 variants should also be considered in the diagnostic evaluation of patients with autosomal dominant HSP. This article is protected by copyright. All rights reserved.
Zur European Journal of Neurology Publikation
- Institute of Clinical Medicine, University of Oslo, Norway.
- Department of Neurology, Oslo University Hospital, Norway.
- Department of Neurology, University of Rostock, Germany.
- German Center for Neurodegenerative Diseases (DZNE), University of Rostock, Germany.
- CeGaT GmbH, Center for Genomics and Transcriptomics, Tübingen, Germany.
- Hertie-Institute for Clinical Brain Research and German Center for Neurodegenerative Diseases (DZNE), University of Tübingen, Germany.
- Department of Medical Genetics, Oslo University Hospital.