Autosomal dominant spondylocostal dysostosis
ORPHA:1797· ICD-10 Q76.4
Definition
A very rare and mild form of spondylocostal dysostosis characterized by vertebral and costal segmentation defects, often with a reduction in the number of ribs.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- No data available