LIU Fuze, WANG Hai. Spinal Stenosis and Thoracolumbar Kyphosis in Achondroplasia[J]. Journal of Rare Diseases, 2023, 2(4): 483-491. DOI: 10.12376/j.issn.2097-0501.2023.04.004
Citation: LIU Fuze, WANG Hai. Spinal Stenosis and Thoracolumbar Kyphosis in Achondroplasia[J]. Journal of Rare Diseases, 2023, 2(4): 483-491. DOI: 10.12376/j.issn.2097-0501.2023.04.004

Spinal Stenosis and Thoracolumbar Kyphosis in Achondroplasia

  • Achondroplasia (ACH) is a rare autosomal-dominant genetic disease resulting from a mutation in the fibroblast growth factor receptor-3 (FGFR3) gene. It is characterized by asymmetric short stature. Spinal stenosis and thoracolumbar kyphosis (TLK) are common findings in ACH patients. Severe TLK can exacerbate spinal stenosis, leading to neurological complications. This paper provides a brief review of the pathophysiological mechanisms, clinical characteristics, and treatments for spinal stenosis and TLK in ACH patients. Recently, three new drugs targeting FGFR3; vosoritide, recifercept, and infigratinib, have completed or are undergoing clinical trials. They have shown promising preliminary results in preventing spinal stenosis and TLK.
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