Key result
Whole exome sequencing links novel biallelic RFC4 variants to severe congenital myopathy in two brothers.
Why the study?
The RFC4 gene was recently linked to Morimoto-Ryu-Malicdan neuromuscular syndrome, but descriptions have been limited to nine patients.
Case Report (n=2)
This case expands the phenotypic spectrum of Morimoto-Ryu-Malicdan neuromuscular syndrome by linking novel biallelic RFC4 variants to severe early-onset axial muscle weakness and hypotonia with preserved intellectual development.
May warrant RFC4 testing in severe congenital myopathy; extends Morimoto-Ryu-Malicdan phenotypic spectrum.
The RFC4 gene has recently been linked to a multisystemic disorder Morimoto-Ryu-Malicdan neuromuscular syndrome, with myopathy being one of the key symptoms described in nine patients. We report the case of two brothers with a rapidly progressive congenital myopathy characterized by severe hypotonia and axial muscle weakness associated with previously unpublished biallelic variants in the RFC4 gene. Whole exome sequencing revealed biallelic variants NM_002916.5:c.1019_1020insCAAA and NM_002916.5:c.982_983insACT, corresponding to the protein-level changes p.(Gly341Lysfs*4) and p.(Thr328delinsAsnSer) in both brothers. This case expands the phenotypic spectrum of Morimoto-Ryu-Malicdan neuromuscular syndrome, highlighting severe early-onset axial muscle weakness, severe hypotonia, and preserved intellectual development. We also provide novel insights into the clinical progression and potential multidisciplinary interventions for patients with Morimoto-Ryu-Malicdan neuromuscular syndrome. Our findings highlight the importance of advanced genetic diagnostics and international collaboration in identifying rare neuromuscular diseases and improving the clinical management of affected patients.
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Lauerová et al. (2025) conducted a case report in Morimoto-Ryu-Malicdan neuromuscular syndrome (n=2). Whole exome sequencing was evaluated on Identification of genetic variants. Whole exome sequencing identified novel biallelic variants in the RFC4 gene in two brothers with rapidly progressive congenital myopathy, severe hypotonia, and axial muscle weakness.
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