Perthes disease in a child with osteogenesis imperfecta from a rare genetic variant: a case report

HIGHLIGHTS

• who: CASE REPORT et al. from the Department of Orthopaedic Surgery, Union, Medical College, Huazhong University of Science and Technology, and Technology, Xianning, China have published the Article: Perthes Disease in a Child With Osteogenesis Imperfecta From a Rare Genetic Variant: A Case Report, in the Journal: (JOURNAL) of 15/04/2022
• what: In contrast, the patient in the study demonstrated classic progression of LCPD, and containment surgery was performed to maintain the femoral head within the acetabulum. The study demonstrated the mutation leading to the abnormal structure or function of collagen type I, resulting . . .
  

   

  

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