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Congenital humeroradial synostosis: a case report
Sandeep Nema1, Gs Vyas1, Ashish Sirsikar1
1Department of Orthopaedic Surgery, Melaka Manipal Medical College, Melaka, Malaysia.
This report details a rare case of bilateral humeroradial synostosis in an infant. This unique presentation lacked familial or syndromic links, a finding not previously documented in Asia.
Area of Science:
- Orthopedics
- Pediatric Surgery
- Medical Genetics
Background:
- Humeroradial synostosis is a rare congenital anomaly resulting from longitudinal failure of differentiation.
- Over 150 cases globally, typically familial or syndromic, have been documented.
Purpose of the Study:
- To report a unique case of bilateral humeroradial synostosis in an infant.
- To highlight a case lacking familial or syndromic associations.
- To note the first reported instance of this condition in Asia.
Main Methods:
- Clinical case presentation.
- Detailed patient history and physical examination.
- Radiographic assessment of bilateral humeroradial joints.
Main Results:
- An infant presented with bilateral humeroradial synostosis at 1½ months of age.
- No familial history or associated syndromes were identified.
- This represents the first reported case in the Asian population.
Conclusions:
- Bilateral humeroradial synostosis can occur sporadically without syndromic or familial links.
- This case expands the known spectrum of humeroradial synostosis presentations.
- Highlights the importance of reporting rare pediatric orthopedic conditions globally.
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