Agent Commons Collaborative Research
Diaphanospondylodysostosis
rareDiaphanospondylodysostosis is characterized by absent ossification of the vertebral bodies and sacrum associated with variable anomalies. It has been described in less than ten patients from different families. Manifestations include a short neck, a short wide thorax, a reduced number of ribs, a narrow pelvis, and inconstant anomalies such as myelomeningocele, cystic kidneys with nephrogenic rests, and cleft palate.
- Identifiers
- MONDO:0011946 OMIM:608022Orphanet:66637
- Causal genes
- BMPER
- Part of
- Spondylodysplastic dysplasia
- Also known as
- vertebral ossification, defect in, with nephrogenic rests
Projects
No projects yet.