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	Franz Bruck	$Bruck syndrome is characterized as the combination of arthrogryposis multiplex congenita and osteogenesis imperfecta. Both diseases are uncommon, but concurrence is extremely rare which makes Bruck syndrome very difficult to research. Bruck syndrome is thought to be an atypical variant of osteogenesis imperfecta most resembling type III, if not its own disease. Multiple gene mutations associated with osteogenesis imperfecta are not seen in Bruck syndrome. Many affected individuals are within the same family, and pedigree data supports that the disease is acquired through autosomal recessive inheritance. Bruck syndrome has features of congenital contractures, bone fragility, recurring bone fractures, flexion joint and limb deformities, pterygia, short body height, and progressive kyphoscoliosis. Individuals encounter restricted mobility and pulmonary function. A reduction in bone mineral content and larger hydroxyapatite crystals are also detectable Joint contractures are primarily bilateral and symmetrical, and most prone to ankles. Bruck syndrome has no effect on intelligence, vision, or hearing. The first case was in 1897 of a male who was described by Franz Bruck as having bone fragility and bone contractures. Franz Bruck was credited with the first description and the disease’s eponym.$ Bruck Syndrome	Brücke's Reagent for Proteins	Brücke Bartley Effect	Ernst Wilhelm Ritter von Brück
Josef Anton Bruckner	Bruckner Society	Józef Polikarp Brudziński	Brudzinski's Meningitis Sign	Brueghel’s Syndrome	Pieter Brueghel the Elder
Pedro Brugada	Brugada Syndrome	Theodor Brugsch	Brugsch's Syndrome	Henri-Louis Roger	Bruit de Roger
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