Key result
A patient with early onset Nemaline myopathy presented with significant craniofacial abnormalities, highlighting the role of surgical and supportive management in addressing anomalous facial growth.
Case Report (n=1)
Highlights the craniofacial manifestations and management considerations in severe nemaline myopathy.
Raises awareness of craniofacial effects in early-onset nemaline myopathy; leaves open optimal management strategies.
Nemaline myopathy (NM) is a rare congenital muscular disease characterized by the presence of rod (nemaline) bodies visualized on muscle biopsy. The disease is genetically and clinically heterogeneous, and the age of onset can vary from neonate to adult. Patients typically present initially with diffuse muscle weakness and hypotonia. The disease also afflicts facial musculature and can cause anomalous facial growth and development. The authors report a patient of early onset NM with significant craniofacial abnormalities. The untreated facial growth is discussed and illustrated in this article. The authors reviewed the current knowledge in the literature regarding the molecular and genetic pathogenesis of NM. The roles of both surgical and supportive management are discussed in this particular patient.
No takes yet. Share an insight, caveat, or question.
Xue et al. (2017) conducted a case report in Nemaline myopathy (n=1). Surgical and supportive management was evaluated. A patient with early onset Nemaline myopathy presented with significant craniofacial abnormalities, highlighting the role of surgical and supportive management in addressing anomalous facial growth.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: