Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene

J Clin Neurosci. 2022 Jun:100:212-213. doi: 10.1016/j.jocn.2022.02.013. Epub 2022 Feb 16.

Authors

Sebastian Boysen¹, Vimala Elumalai¹, Reem H ElSheikh¹, Akilandeswari Aravindhan¹, Aravindhan Veerapandiyan²

Affiliations

¹ Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
² Division of Neurology, Department of Pediatrics, Arkansas Children's Hospital, University of Arkansas for Medical Sciences, Little Rock, AR, USA. Electronic address: aveerapandiyan@uams.edu.

PMID: 35181192
DOI: 10.1016/j.jocn.2022.02.013

No abstract available

Keywords: HSP; Hereditary spastic paraplegia; IGE; Idiopathic generalized epilepsy; NIPA1; SPG6; Spastic paraplegia 6.

Publication types

Letter
Comment

MeSH terms

Epilepsy* / complications
Epilepsy* / genetics
Humans
Membrane Proteins / genetics
Mutation / genetics
Pedigree
Spastic Paraplegia, Hereditary* / complications
Spastic Paraplegia, Hereditary* / genetics

Substances

Membrane Proteins
NIPA1 protein, human