Bruck syndrome is characterized by the association of osteogenesis imperfecta and congenital joint contractures.
Comprehensive, easy-to-understand information about this condition
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European rare disease database
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.