Developmental dysplasia of the hip (DDH) is one of the most common causes of disability in children (
1). This condition results from a developmental defect in the positioning of the femoral head within the hip joint and its surrounding ligaments. Although various pathological factors can lead to this phenomenon, the exact etiology of the disease remains unclear (
2). DDH can cause a wide range of disabilities, with its incidence varying geographically, being lowest in South Africa and highest among Native Americans and Caucasians. The overall incidence has been reported to range from 0.6 to 1.1 per 1000 live births, and 30% of total hip joint replacements have been associated with this condition (
3). Early diagnosis in childhood allows for non-surgical treatment. However, delayed diagnosis, lack of appropriate treatment, or treatment failure can lead to complications, such as premature osteoarthritis, secondary femoral injuries, and movement disorders, potentially necessitating total hip joint replacement (
4). Total hip arthroplasty (THA) is a surgical technique for correcting DDH (
5-
7). Various THA-based techniques have been developed for managing end-stage osteoarthritis in Crowe DDH type III or IV patients. The primary goal is to achieve long-term stability of the acetabulum by ensuring excellent cap coverage and correctly positioning the hip joint rotation center. Placing the acetabular component in the true acetabulum is considered ideal biomechanically and biologically (
8). Femoral shortening, introduced by Eskelinen et al., is a complementary method for THA to address contractions and reduce pressure on the hip joint without stretching the sciatic nerve (
9,
10). Several studies have assessed the long-term outcomes of THA for DDH using shortening subtrochanteric osteotomy (STO) (
10-
15). However, this approach remains challenging, as incompatibility between the diameters of the proximal and distal canals post-shortening STO can lead to difficulties in achieving lasting and secure fixation, increasing the risk of delayed bone healing, malunion, or nonunion (
5,
12,
16-
19). Additional complications include nerve palsy (
17-
21), femoral fractures during surgery (
12,
16,
22), and dislocation (
12,
18,
19,
21). Although various THA-based surgical techniques for end-stage osteoarthritis in DDH Crowe type III or IV patients have been introduced, no gold standard has been established for THA surgery, and study results remain inconsistent (
23,
24).