A rare case of the complex phenotype of hereditary spastic paraparesis due to a mutation in a novel gene variant

Hereditary spastic paraplegia (HSP), is a heterogeneous group of corticospinal tract disorders leading to progressive lower limb weakness and spasticity. Recessive mutations in DDHD2 characteristically involve early onset delay in motor and cognitive milestones coupled with spasticity. The complex n...

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Bibliographic Details

Published in:	Journal of Current Research in Scientific Medicine
Main Authors:	B Jude Antonieo Raja, Sakthi Abirami, Priya Jose, Peter Prasanth Kumar Kommu
Format:	Article
Language:	English
Published:	Wolters Kluwer Medknow Publications 2022-01-01
Subjects:	autosomal recessive cerebral palsy ddhd2 hereditary spastic paraplegias phospholipases
Online Access:	http://www.jcrsmed.org/article.asp?issn=2455-3069;year=2022;volume=8;issue=2;spage=206;epage=208;aulast=Antonieo