Rare Diseases Symptoms Automatic Extraction

A novel splicing mutation in COL1A1 gene caused type I osteogenesis imperfecta in a Chinese family.

[dentinogenesis imperfecta]

Osteogenesis imperfect (OI) is a heritable connective tissue disorder with bone fragility as a cardinal manifestation, accompanied by short stature, dentinogenesis imperfecta, hyperlaxity of ligaments and skin, blue sclerae and hearing loss. Dominant form of OI is caused by mutations in the type I procollagen genes, COL1A1/A2. Here we identified a novel splicing mutation c.3207+1G>A (GenBank ID: JQ236861) in the COL1A1 gene that caused type I OI in a Chinese family. RNA splicing analysis proved that this mutation created a new splicing site at c.3200, and then led to frameshift. This result further enriched the mutation spectrum of type I procollagen genes.

Diseases presenting "dentinogenesis imperfecta" symptom

  • dentin dysplasia
  • dentinogenesis imperfecta
  • oligodontia
  • papillon-lefèvre syndrome

This symptom has already been validated