Rare Diseases Symptoms Automatic Extraction

Osteogenesis imperfecta/lobstein syndrome associated with dentinogenesis imperfecta.

[dentinogenesis imperfecta]

Osteogenesis imperfecta is a collagen related disorder characterized by increased bone fragility and low bone mass. The important oral finding in osteogenesis imperfect is the presence of dentinogenesis imperfecta. This article presents a case of osteogenesis imperfecta (type IV B) with dentinogenesis imperfecta where a 7-year-old girl had opalacent primary teeth associated with severe bone deformity, scoliosis, barrel shaped rib cage, and short stature. The clinical, radiographic ad histologic features are reviewed along with management aspects.

Diseases presenting "scoliosis" symptom

  • achondroplasia
  • alexander disease
  • cadasil
  • cohen syndrome
  • dentinogenesis imperfecta
  • gm1 gangliosidosis
  • holt-oram syndrome
  • homocystinuria without methylmalonic aciduria
  • proteus syndrome
  • thoracic outlet syndrome

This symptom has already been validated