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Objective: To compare prevalence and severity of sacral dysmorphism in Indigenous and non-Indigenous Australian populations.
Methods: We performed a single centre retrospective matched cohort study in consecutive Indigenous and non-Indigenous Australian patients who received a CT scan of the pelvis between January and March 2024 at our institution. Patients were excluded if they were under the age of 18 at the time of the scan or had a history of pelvic fractures or fixation. CT scans were assessed for both qualitative and quantitative features of sacral dysmorphism. The primary outcome of interest was the prevalence and severity of sacral dysmorphism in Indigenous and non-Indigenous Australian populations.
Results: 120 patients were included in the study - 60 Indigenous and 60 non-Indigenous Australians. All patients exhibited at least one characteristic of sacral dysmorphism. There was no difference in the prevalence of qualitative sacral dysmorphism between the two groups. Compared to their non-Indigenous counterpart, Indigenous patients demonstrated a lower S1 transsacral corridor coronal diameter (20.50 vs. 21.85 mm, p = 0.005), S1 oblique corridor axial diameter (17.90 vs. 19.60 mm, p = 0.028), S1 pelvic width (144.85 vs. 158.70 mm, p < 0.001), S2 transsacral corridor coronal diameter (13.70 vs. 14.95 mm, p = 0.013), S2 transsacral corridor axial diameter (10.60 vs. 11.55 mm, p = 0.013), and S2 pelvic width (126.60 vs 136.00 mm, p < 0.001). Additionally, in Indigenous patients, S1 and S2 transsacral and oblique S1 iliosacral fixation lengths were shorter. Where an S1 trans-sacral osseous corridor was not present, the S2 corridor was significantly larger in coronal, axial measurements across both groups (p < 0.001).
Conclusions: Indigenous Australian patients exhibited more severe forms of sacral dysmorphism when compared to their non-Indigenous counterparts. Additionally the overall prevalence of sacral dysmorphism across this Australian population was amongst the highest reported in the literature. This may present significant technical challenges and warrants consideration when performing percutaneous iliosacral screw fixation.
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http://dx.doi.org/10.1016/j.injury.2025.112667 | DOI Listing |
Injury
October 2025
Department of Orthopaedic Surgery, The Royal Adelaide Hospital, Adelaide, South Australia, Australia; Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia.
Objective: To compare prevalence and severity of sacral dysmorphism in Indigenous and non-Indigenous Australian populations.
Methods: We performed a single centre retrospective matched cohort study in consecutive Indigenous and non-Indigenous Australian patients who received a CT scan of the pelvis between January and March 2024 at our institution. Patients were excluded if they were under the age of 18 at the time of the scan or had a history of pelvic fractures or fixation.
Int J Surg Case Rep
September 2025
Orthopedic Surgery Specialist, Damascus Hospital, Syria.
Introduction And Importance: Congenital anomalies remain a significant global health challenge, affecting 6 %-8 % of newborns worldwide and contributing to high rates of infant mortality and disability. This case report presents a unique constellation of congenital malformations in a six-year-old male born to consanguineous parents with a family history of metabolic disorders, including maternal diabetes and paternal smoking-both known risk factors for birth defects.
Case Presentation: The patient exhibited a complex phenotype including rib agenesis, hydrocephalus, sacral agenesis, atrial septal defect, and severe lower limb deformities characterized by complete tibial absence on the right and a 180-degree rotational malalignment of the left tibia and fibula.
We report a rare case of an asymptomatic persistent sciatic artery (PSA) detected on Doppler ultrasonography (DUS) in a boy with SACRAL syndrome. We describe the natural course of PSA and emphasize the importance of repeated DUS, which is the preferred imaging modality by vascular physicians, in identifying anatomical features and variations in malformative syndromes.
View Article and Find Full Text PDFBMJ Case Rep
July 2025
General Surgery, All India Institute of Medical Sciences Kalyani, Kalyani, West Bengal, India.
Neurofibromatosis type 1 (NF1) is a genetic disorder characterised by neurofibromas and skeletal anomalies, including lumbar kyphoscoliosis and dysmorphic sacral vertebrae. We report a rare case of a male in his late 30s with NF1 presenting with a left-sided hip dislocation and an unusual response to spinal anaesthesia. Spinal anaesthesia was attempted using 3 mL of 0.
View Article and Find Full Text PDFEur J Orthop Surg Traumatol
July 2025
Department of Trauma Surgery, University of Zurich, University Hospital of Zurich, Zurich, Switzerland.
Purpose: Navigated sacroiliac screw fixation of the posterior pelvic ring has been introduced, providing the surgeon with an improved three-dimensional orientation of the anatomy. The primary aim of this study was to evaluate the influence of navigation on the surgical outcome. The secondary aim was to evaluate the relevance of sacral dysmorphism.
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