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A rare case of pelvic bone duplication.
Lamya Ann Atweh1, Abdo Jurjus2, Nassif Farah3
1Department of Diagnostic Radiology, American University of Beirut, Beirut, Lebanon.
Skeletal Radiology
|February 16, 2018
Summary
This study presents a rare case of iliac bone duplication in a 5-month-old infant. The findings explore potential genetic and epigenetic causes for this pelvic malformation.
Area of Science:
- Developmental biology
- Orthopedic surgery
- Medical genetics
Background:
- Pelvic girdle development is a complex process influenced by genetic and epigenetic factors.
- Iliac bone malformations are infrequent congenital anomalies.
- Understanding the etiology of these malformations is crucial for diagnosis and management.
Observation:
- A 5-month-old male infant presented with a rare iliac bone malformation.
- The malformation involved a duplication of the ilium.
- Detailed clinical and imaging data were collected.
Findings:
- The case highlights a unique instance of iliac duplication.
- Potential genetic and epigenetic disturbances are proposed as causative factors.
- This finding contributes to the understanding of rare skeletal dysplasias.
Implications:
- This case provides insights into the developmental pathways of the pelvic girdle.
- Further research into the genetic underpinnings of iliac malformations is warranted.
- Improved understanding may lead to earlier diagnosis and targeted interventions for similar rare conditions.
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