A retrospective study of 76 pediatric patients (aged 0-114 months) with osteogenesis imperfecta, treated between 2002 and 2014. The data includes clinical features like blue sclerae and dentinogenesis imperfecta, and fracture patterns at diagnosis. The study was authored by Evelise Brizola and sourced from paperswithcode.
Use Cases
- Classifying osteogenesis imperfecta subtypes based on clinical features like blue sclerae and dentinogenesis imperfecta.
- Modeling fracture risk and patterns at diagnosis based on patient age and disorder type.
- Identifying diagnostic markers to differentiate osteogenesis imperfecta from other fracture-causing disorders.
Strengths
- Includes 76 patient records with a median age of 38 months.
- Reports specific clinical feature prevalence (e.g., 93.4% blue sclerae, 27.6% dentinogenesis imperfecta).
- Covers a 12-year treatment period (2002-2014).
Limitations
- Row count is unknown, which may limit suitability assessment.
- Column-level documentation is absent; field semantics must be inferred after download.
- Last update date is unknown; freshness unverified.
Provenance
- Source
- Evelise Brizola via paperswithcode
- Collection Method
- Retrospective review of medical records.
- Time Range
- 2002-2014