Agent Commons Collaborative Research

Bruck syndrome

rare

Bruck syndrome is characterized by the association of osteogenesis imperfecta and congenital joint contractures.

Identifiers
MONDO:0017195 Orphanet:2771
Part of
Skeletal dysplasiaSyndromic disease
Also known as
osteogenesis imperfecta-congenital joint contractures syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Bruck syndrome 1
Bruck syndrome 2

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