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 dysplasia Syndromic disease
Also known as: osteogenesis imperfecta-congenital joint contractures syndrome

Subtypes

Disease	ID	Subtypes	Genes
Bruck syndrome 1	MONDO:0009806		FKBP10
Bruck syndrome 2	MONDO:0012217		PLOD2

Rare disease

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