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The article presents a case report of a 13-year-old boy diagnosed with Beals syndrome, a rare autosomal-dominant connective tissue disorder characterized by multiple flexion contractures and other features similar to Marfan syndrome. The patient presented with fractures of the distal tibia and fibula, a finding not previously documented in relation to Beals syndrome. The report highlights the need for further studies to explore the potential association between Beals syndrome and an increased incidence of f

Author

abuseifdoha995

Language

EN