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Up to: Skeletal dysplasia

Spondylometaphyseal dysplasia

Spondylometaphyseal dysplasias are a heterogeneous group of disorders associated with walking and growth disturbances that become evident during the second year of life.

0 trials tagged with this condition →

  • Kniest dysplasia 0 trials
  • SBDS-related severe neonatal spondylometaphyseal dysplasia 0 trials
  • Spondyloenchondrodysplasia with immune dysregulation 0 trials
  • Autosomal recessive spondylometaphyseal dysplasia, Megarbane type 0 trials
  • Axial spondylometaphyseal dysplasia 0 trials
  • Odontochondrodysplasia 0 trials Sub-types →
  • Regressive spondylometaphyseal dysplasia 0 trials
  • Spondyloepimetaphyseal dysplasia, Strudwick type 0 trials
  • Spondylometaphyseal dysplasia, 'corner fracture' type 0 trials
  • Spondylometaphyseal dysplasia, A4 type 0 trials
  • Spondylometaphyseal dysplasia, Czarny-Ratajczak type 0 trials
  • Spondylometaphyseal dysplasia, East African type 0 trials
  • Spondylometaphyseal dysplasia, Golden type 0 trials
  • Spondylometaphyseal dysplasia, Kozlowski type 0 trials
  • Spondylometaphyseal dysplasia, Schmidt type 0 trials
  • Spondylometaphyseal dysplasia, Sedaghatian type 0 trials
  • Spondylometaphyseal dysplasia, pagnamenta type 0 trials
  • Spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome 0 trials
  • Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome 0 trials

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