Human Genome Variation (Mar 2024)

Ventriculosubgaleal shunt placement for hydrocephalus in osteogenesis imperfecta with novel compound heterozygous CRTAP variants

  • Shintaro Nakamura,
  • Kyosuke Ibi,
  • Hiroyuki Tanaka,
  • Hirokazu Takami,
  • Keita Okada,
  • Nao Takasugi,
  • Motohiro Kato,
  • Naoto Takahashi,
  • Takanobu Inoue

DOI
https://doi.org/10.1038/s41439-024-00274-z
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 4

Abstract

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Abstract Osteogenesis imperfecta is characterized by frequent fractures, bone deformities, and other systemic symptoms. Severe osteogenesis imperfecta may progress to hydrocephalus; however, treatment strategies for this complication remain unclear. Here, we describe severe osteogenesis imperfecta in an infant with symptomatic hydrocephalus treated with ventriculosubgaleal shunt placement. Targeted next-generation sequencing revealed novel compound heterozygous CRTAP variants, i.e., NM_006371.5, c.241 G > T, p.(Glu81*) and NM_006371.5, c.923-2_932del. We suggest that ventriculosubgaleal shunt placement is an effective and safe treatment for hydrocephalus in patients with severe osteogenesis imperfecta.