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199 Possible Causes for Diffuse Osseous Demineralization, Severe Progressive Kyphoscoliosis

  • Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations
  • Spondylolisthesis

    A 12-year-old boy with Hunter syndrome presented with severe thoracolumbar kyphoscoliosis and no associated symptoms.[] The deformity progressed to kyphosis of 60 and scoliosis of 42 prior to surgical intervention.[]

    Missing: Diffuse Osseous Demineralization
  • Joint Subluxation

    However, deformity in patients with the kyphoscoliosis type may be particularly severe and develop after rapid progression.[] Kyphoscoliosis Type The kyphoscoliosis type is characterized by severe hypotonia and scoliosis ( Table 1 ). Inheritance is autosomal recessive.[] Jasiewicz et al 28 reviewed 11 patients with EDS who underwent surgical treatment of kyphoscoliosis.[]

    Missing: Diffuse Osseous Demineralization
  • Renal Pelvic Calculus

    CONCLUSION RTS is a rare genetic condition which landmark is kyphoscoliosis, often progressive during the adolescent growth.[] It can produce severe thoracic 13 Bounakis N, Karampalis C, Sharp H, Tsirikos AI. Surgical treatment of scoliosis in Rubinstein-Taybi syndrome type 2.[]

    Missing: Diffuse Osseous Demineralization
  • Cold-Induced Sweating Syndrome Type 1

    Management and treatment Surviving patients usually develop severe progressive kyphoscoliosis that requires corset therapy or corrective surgery.[]

    Missing: Diffuse Osseous Demineralization
  • Ectopia Lentis

    ., 1994: Mol Cell Probes 8:325-327; Furthmayr and Francke, 1997: Semin Thorac Cardiovasc Surg 9:191-205], and severe progressive kyphoscoliosis [Adès et al., 2002: Am J Med[] progressive kyphoscoliosis, the ‘MASS’ phenotype (myopia, mitral valve prolapse, borderline aortic root enlargement, skin and skeletal findings), mitral valve prolapse syndrome[] 12 Mutations in this gene result in classical MFS, neonatal MFS, autosomal dominant ascending aortic aneurysms, familial arachnodactyly, Shprintzen–Goldberg syndrome and severe[]

    Missing: Diffuse Osseous Demineralization
  • Kyphoscoliosis

    To our knowledge, this is the first report of a family with an FBN1 gene mutation cosegregating with an unusual autosomal dominant progressive kyphoscoliosis of variable severity[] People with kyphoscoliosis that is moderate, severe or progressive do benefit from medical care.[] CONCLUSIONS: Congenital kyphosis and kyphoscoliosis are uncommon deformities with the potential to progress rapidly, resulting in severe deformity and possible neurological[]

    Missing: Diffuse Osseous Demineralization
  • Anuria

    CONCLUSION: In this spina bifida patient, who had reached the age of 35 years, severe kyphoscoliosis and lack of vascular access presented insurmountable challenges to implement[] However, the patient expired 19 days later due to progressive respiratory failure.[]

    Missing: Diffuse Osseous Demineralization
  • Arthrogryposis Multiplex Congenita

    症例報告 治療に難渋した先天性多発性関節拘縮症に伴う脊柱後側弯症の1例 A Severe Progressive Kyphoscoliosis Secondary to Arthrogryposis Multiplex Congenita.[] We report a case of arthrogryposis multiplex congenita (AMC) complicated by severe progressive kyphoscoliosis. [] A 14-year-old girl with AMC presented with a severe progressive trunk deformity and was referred to our clinic. []

    Missing: Diffuse Osseous Demineralization
  • Warburg Micro Syndrome 3

    Radiological examination of the skeleton showed a left curved scoliosis, convex vertebral bodies, diffuse osseous demineralization, thin diaphyses of the long bones, bilateral[]

    Missing: Severe Progressive Kyphoscoliosis

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