A Severe Form of Familial Desminopathy Due to a Homozygous Nonsense DES Variant in Two Siblings

Neuropediatrics. 2023 Aug;54(4):279-286. doi: 10.1055/a-1871-3692. Epub 2022 Jun 8.

Abstract

Familial primary desminopathies are usually autosomal dominantly inherited and present at the age of 20 to 40 years with progressive muscle weakness and atrophy, cardiomyopathy, and cardiac arrhythmias. Cardiac features may precede the muscular weakness. Here, we report the rare case of two siblings presenting with a desminopathy at pediatric age, due to homozygous nonsense variations (c.700G > T [p.Glu234Ter]) in DES, representing an autosomal recessive inheritance pattern. The homozygous state of these variants is expected to result in the complete absence of desmin production. Rare autosomal recessive DES variants are associated with an earlier clinical presentation (from childhood to early adulthood) and faster evolution compared with more common autosomal dominant variants. A normal resting electrocardiography (ECG) and cardiac ultrasound can be a pitfall, as seen in our patient who has extensive fibrotic scarring on cardiac magnetic resonance imaging (MRI). We recommend yearly cardiac ultrasound, yearly 24-hour Holter monitoring and 2 yearly cardiac MRI from the age of 10 years in all asymptomatic patients. Heterozygous patients usually have no or only mild complaints but, though not yet reported in autosomal recessive desminopathies, muscular complaints are possible, as seen in the father of our patients. The prognosis for these patients with desminopathy presenting in childhood is unpredictable but anticipated as poor.

MeSH terms

  • Adult
  • Cardiomyopathies* / diagnostic imaging
  • Cardiomyopathies* / genetics
  • Cardiomyopathies* / pathology
  • Child
  • Electrocardiography
  • Heterozygote
  • Homozygote
  • Humans
  • Siblings*
  • Young Adult