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  3. Research By Disease

Disease: Ankle defects short stature

  • <em>CTCF</em>-Related Disorder
  • A case of mesomelic dysplasia Kantaputra type--new findings and a new diagnostic approach
  • Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature
  • Are parents of children with Cockayne syndrome manifesting features of the disorder?: Case reports
  • Axial correction of the lower limb deformities in a girl with anauxetic dysplasia
  • Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome
  • Combined tarsal and carpal tunnel syndrome in mucolipidosis type III. A case study and review
  • Corrections of lower limb deformities in patients with diastrophic dysplasia
  • Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan
  • Marjolin's Ulcer in Laron Syndrome - an Unexpected Combination: A Case Report
  • Marked variability in the radiographic features of cartilage-hair hypoplasia: case report and review of the literature
  • Schmid's Type of Metaphyseal Chondrodysplasia: Diagnosis and Management
  • Spondyloepimetaphyseal dysplasia with joint laxity type 2: Aggregating the literature and reporting on the life of a 66-year-old man
  • The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study
  • Troyer Syndrome
  • Two-stage Bone Lengthening With Reuse of a Single Intramedullary Telescopic Nail in Patients With Achondroplasia
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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