These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
113 related articles for article (PubMed ID: 32612477)
1. A Rare Case of Bruck Syndrome Type 2 in Siblings With Broad Phenotypic Variability. Luce L; Casale M; Waldron S Ochsner J; 2020; 20(2):204-208. PubMed ID: 32612477 [No Abstract] [Full Text] [Related]
2. Novel Mutations in PLOD2 Cause Rare Bruck Syndrome. Lv F; Xu X; Song Y; Li L; Asan ; Wang J; Yang H; Wang O; Jiang Y; Xia W; Xing X; Li M Calcif Tissue Int; 2018 Mar; 102(3):296-309. PubMed ID: 29177700 [TBL] [Abstract][Full Text] [Related]
3. Bruck syndrome: a rare combination of bone fragility and multiple congenital joint contractures. Breslau-Siderius EJ; Engelbert RH; Pals G; van der Sluijs JA J Pediatr Orthop B; 1998 Jan; 7(1):35-8. PubMed ID: 9481655 [TBL] [Abstract][Full Text] [Related]
8. The first case of Bruck syndrome associated with gastroschisis. Afşarlar ÇE; Peltek-Kendirci HN; Erdoğan D; Özgüner İF; Çavuşoğlu YH; Karaman A; Çetinkaya S Turk J Pediatr; 2013; 55(6):651-4. PubMed ID: 24577988 [TBL] [Abstract][Full Text] [Related]
9. Expanding the phenotype of Bruck syndrome: Severe limb deformity, arthrogryposis, congenital cardiac disease and pulmonary hemorrhage. Sandy JL; Perez D; Goh S; Forsey J; Rajagopalan S; Trivedi A; Munns CF Am J Med Genet A; 2023 Jan; 191(1):265-270. PubMed ID: 36282022 [TBL] [Abstract][Full Text] [Related]
10. Osteogenesis imperfecta with joint contractures: bruck syndrome. Blacksin MF; Pletcher BA; David M Pediatr Radiol; 1998 Feb; 28(2):117-9. PubMed ID: 9472060 [TBL] [Abstract][Full Text] [Related]
11. Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2. Ha-Vinh R; Alanay Y; Bank RA; Campos-Xavier AB; Zankl A; Superti-Furga A; Bonafé L Am J Med Genet A; 2004 Dec; 131(2):115-20. PubMed ID: 15523624 [TBL] [Abstract][Full Text] [Related]
12. Bruck syndrome - a rare syndrome of bone fragility and joint contracture and novel homozygous FKBP10 mutation. Moravej H; Karamifar H; Karamizadeh Z; Amirhakimi G; Atashi S; Nasirabadi S Endokrynol Pol; 2015; 66(2):170-4. PubMed ID: 25931047 [TBL] [Abstract][Full Text] [Related]
13. Arthrogryposis multiplex congenita in a child with congenital fractures: a case report. Dayasiri K; Jayaweera H J Med Case Rep; 2022 Oct; 16(1):376. PubMed ID: 36258204 [TBL] [Abstract][Full Text] [Related]
14. Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta. Steinlein OK; Aichinger E; Trucks H; Sander T BMC Med Genet; 2011 Nov; 12():152. PubMed ID: 22107750 [TBL] [Abstract][Full Text] [Related]
17. Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome)--evidence for possible autosomal recessive inheritance. Brady AF; Patton MA Clin Dysmorphol; 1997 Oct; 6(4):329-36. PubMed ID: 9354841 [TBL] [Abstract][Full Text] [Related]
18. Bruck syndrome (osteogenesis imperfecta with congenital joint contractures): review and report on the first North American case. McPherson E; Clemens M Am J Med Genet; 1997 May; 70(1):28-31. PubMed ID: 9129737 [TBL] [Abstract][Full Text] [Related]
19. Bruck syndrome in 13 new patients: Identification of five novel FKBP10 and PLOD2 variants and further expansion of the phenotypic spectrum. Otaify GA; Abdel-Hamid MS; Hassib NF; Elhossini RM; Abdel-Ghafar SF; Aglan MS Am J Med Genet A; 2022 Jun; 188(6):1815-1825. PubMed ID: 35278031 [TBL] [Abstract][Full Text] [Related]