Ontology highlight
ABSTRACT:
SUBMITTER: Nakamura S
PROVIDER: S-EPMC10978965 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature

Human genome variation 20240328 1
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 ...[more]