Skip to content

1 paper indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Case report Sep 2026

A rare case of hereditary spastic paraplegia with homozygous mutation in the ZFYVE26 gene.

Hereditary spastic paraplegia (HSP) refers to a group of rare, progressive neurodegenerative disorders characterized by spasticity and weakness predominantly affecting the lower limbs, with significant clinical and genetic heterogeneity. Clinically, HSP is classified into "pure" and "complicated" forms. SPG15 (ZFYVE26)...

Betül Özenç, D. D. Oge, Pelin Yenilmez Yeşildaş · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.