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Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69.

Neurogenetics - 28 Nov 2024

Sadr Zahra, Ghasemi Aida, Rohani Mohammad, Khorram Khorshid Hamid Reza, Habibi-Kavashkohie Mohammad Reza, Mohammadi Yusuf, Alavi Afagh

Abstract excerpt

Some subtypes of hereditary spastic paraplegia (HSP), especially with autosomal recessive inheritance (AR-HSP), have been reported rarely. In this study, we report the clinical features and molecular results of three unrelated Iranian patients with rare subtypes of HSP, including SPG76, SPG56, and SPG69; thereafter, we compare them to other reported cases. Three patients who were clinically diagnosed with HSP and...

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PMID: 39607444
DOI: 10.1007/s10048-024-00789-1

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