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RARS1-related hypomyelinating leukodystrophy-9 (HLD-9) in two distinct Iranian families: Case report and literature review.

Sajjad BiglariHassan VahidnezhadMohammad Amin TabatabaiefarHamid Reza Khorram KhorshidEmran Esmaeilzadeh
Published in: Molecular genetics & genomic medicine (2024)
Pathogenic variants in RARS1 decrease ArgRS activity and cause a wide range of symptoms, from severe, early onset epileptic encephalopathy with brain atrophy to a mild condition with relatively maintained myelination. These symptoms include the classic hypomyelination presentation with nystagmus and spasticity. Furthermore, the pathogenicity of the variation c.2T>C (p.Met1Thr) has been shown.
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