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- Bruck_syndrome abstract "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.".
- Bruck_syndrome wikiPageID "42309316".
- Bruck_syndrome wikiPageLength "10265".
- Bruck_syndrome wikiPageOutDegree "13".
- Bruck_syndrome wikiPageRevisionID "707348778".
- Bruck_syndrome wikiPageWikiLink Arthrogryposis.
- Bruck_syndrome wikiPageWikiLink Category:Abnormalities_of_dermal_fibrous_and_elastic_tissue.
- Bruck_syndrome wikiPageWikiLink Category:Genetic_disorders.
- Bruck_syndrome wikiPageWikiLink Category:Orthopaedic_eponyms.
- Bruck_syndrome wikiPageWikiLink Category:Rare_diseases.
- Bruck_syndrome wikiPageWikiLink Category:Skeletal_disorders.
- Bruck_syndrome wikiPageWikiLink Congenital_disorder.
- Bruck_syndrome wikiPageWikiLink Contracture.
- Bruck_syndrome wikiPageWikiLink Hydroxylapatite.
- Bruck_syndrome wikiPageWikiLink Kyphoscoliosis.
- Bruck_syndrome wikiPageWikiLink Osteogenesis_imperfecta.
- Bruck_syndrome wikiPageWikiLink Pterygium.
- Bruck_syndrome wikiPageWikiLink Telopeptide.
- Bruck_syndrome wikiPageWikiLinkText "Bruck syndrome".
- Bruck_syndrome wikiPageUsesTemplate Template:Reflist.
- Bruck_syndrome subject Category:Abnormalities_of_dermal_fibrous_and_elastic_tissue.
- Bruck_syndrome subject Category:Genetic_disorders.
- Bruck_syndrome subject Category:Orthopaedic_eponyms.
- Bruck_syndrome subject Category:Rare_diseases.
- Bruck_syndrome subject Category:Skeletal_disorders.
- Bruck_syndrome comment "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.".
- Bruck_syndrome label "Bruck syndrome".
- Bruck_syndrome sameAs Q3508623.
- Bruck_syndrome sameAs Syndrome_de_Bruck.
- Bruck_syndrome sameAs m.0y4y_q6.
- Bruck_syndrome sameAs Q3508623.
- Bruck_syndrome wasDerivedFrom Bruck_syndrome?oldid=707348778.
- Bruck_syndrome isPrimaryTopicOf Bruck_syndrome.