Why the study?
There were no reported cases of gene-based therapy in rare patients with 5q SMA caused by subtle SMN1 variants of unknown clinical significance.
What are the clinical features, genetic profiles, and responses to gene-based therapy in rare patients with 5q SMA caused by intragenic SMN1 variants combined with a heterozygous deletion?
Cohort (n=10)
What are the clinical features, genetic profiles, and responses to gene-based therapy in rare patients with 5q SMA caused by intragenic SMN1 variants combined with a heterozygous deletion?
Answers are grounded in this paper and cite their sources.
Gene-based therapy in rare 5q SMA patients with intragenic SMN1 variants and heterozygous deletion shows results consistent with those in typical homozygous deletion patients.
Spinal muscular atrophy 5q (5q SMA) is one of the most prevalent autosomal recessive disorders globally. The underlying cause of 5q SMA is attributed to variants in SMN1. To date, there are no reported cases of gene-based therapy in rare patients with 5q SMA caused by subtle SMN1 variants of unknown clinical significance. We included 10 patients with the clinical manifestations of 5q SMA associated with intragenic variants in combination with a heterozygous SMN1 deletion in this retrospective study. Previously reported pathogenic or likely pathogenic variants were identified (e.g., c.*3+1del, c.815A>G (p.Tyr272Cys), and c.821C>T (p.Thr274Ile)). Variants of unknown clinical significance were also found, including a recurrent, previously unreported variant c.80A>C (p.Gln27Pro). We also report detailed molecular genetic and clinical data on 9 patients with 5q SMA. In addition, we provide results from the cohort of patients with gene-based therapy, consistent with data from patients with a homozygous SMN1 deletion.
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Mikhalchuk et al. (2026) conducted a cohort in Spinal muscular atrophy 5q (5q SMA) (n=10). Gene-based therapy vs. Homozygous SMN1 deletion patients was evaluated.
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