Key result
De novo ACTA1 variant linked to severe neonatal congenital myopathy and fatal respiratory failure.
Why the study?
ACTA1-related congenital myopathies are rare neuromuscular disorders with significant genotypic heterogeneity, presenting diagnostic and management challenges in severe neonatal cases.
Case Report (n=1)
No
This case highlights the clinical overlap between ACTA1 myopathy and perinatal asphyxia, emphasizing the need for genetic testing in hypotonic neonates with atypical presentations.
Adds novel lethal ACTA1 variant to literature; leaves open genotype-phenotype correlations and optimal management in neonatal myopathy.
Background ACTA1 -related congenital myopathies are rare neuromuscular disorders with significant genotypic heterogeneity, often causing severe neonatal multisystem involvement. This study presents a severe neonatal case with a pathogenic ACTA1 variant and reviews literature to highlight diagnostic and management challenges. Case presentation A female infant was born via cesarean section at 39 +1 weeks to a non-consanguineous mother. Prenatal ultrasound showed polyhydramnios. She presented with severe birth asphyxia (Apgar 3 at 1 min, 5 at 5 min), requiring immediate resuscitation. Physical examination revealed profound hypotonia, absent spontaneous movements, respiratory insufficiency necessitating mechanical ventilation, expressionless facies, and bulbar dysfunction. Laboratory tests indicated metabolic acidosis and elevated lactate and creatine kinase. Electromyography (EMG) demonstrated reduced motor amplitudes and spontaneous fibrillations. Whole-exome sequencing identified a de novo heterozygous pathogenic variant in ACTA1 (c.227G>A, p. Gly76Asp), confirming ACTA1 -related congenital myopathy. Care was withdrawn on day 18 due to poor neurologic recovery. Conclusion This case highlights three critical implications: (1) the significant clinical overlap between ACTA1 myopathy and perinatal asphyxia, underscoring the necessity of genetic testing in hypotonic neonates with atypical presentations; (2) the grave prognosis of early-onset ACTA1 mutations, which mandates early palliative care consultation; and (3) the essential role of a precise genetic diagnosis in defining phenotypes and informing future targeted therapies, such as gene therapy.
No takes yet. Share an insight, caveat, or question.
Zhao et al. (2026) conducted a case report in ACTA1-related congenital myopathy (n=1). ACTA1 mutation (c.227G>A, p.Gly76Asp) was evaluated on Clinical outcome. A de novo pathogenic variant in ACTA1 (c.227G>A, p.Gly76Asp) resulted in severe neonatal congenital myopathy characterized by profound hypotonia and respiratory failure, leading to death on day 18.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: