Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population

Genes (Basel). 2021 Nov 10;12(11):1783. doi: 10.3390/genes12111783.

Abstract

Congenital myopathies are rare neuromuscular hereditary disorders that manifest at birth or during infancy and usually appear with muscle weakness and hypotonia. One of such disorders, early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD, OMIM: 614399, MIM: 612453), is a rare autosomal recessive disorder caused by biallelic mutations (at homozygous or compound heterozygous status) in MEGF10 (multiple epidermal growth factor-like domains protein family). Here, we report two unrelated patients, who were born to consanguineous parents, having two novel MEGF10 deleterious variants. Interestingly, the presence of MEGF10 associated EMARDD has not been reported in Saudi Arabia, a highly consanguineous population. Moreover, both variants lead to a different phenotypic onset of mild and severe types. Our work expands phenotypic features of the disease and provides an opportunity for genetic counseling to the inflicted families.

Keywords: MEGF10; atelectasis; bronchiectasis; butterfly vertebrae; congenital myopathy; convex scoliosis; flexion deformity; novel variants; splicing; subluxation.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Consanguinity
  • Humans
  • Infant
  • Male
  • Membrane Proteins / genetics*
  • Myotonia Congenita / genetics*
  • Myotonia Congenita / pathology
  • Pedigree
  • Phenotype*

Substances

  • MEGF10, human
  • Membrane Proteins