- A Case of Osteogenesis Imperfecta: Diagnosed in Uterus by Ultrasonogram
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Kim JS, Kang JB, Huh JS, Kim HB, Lee KY, Kang SW, Park KJ
- KMID: 2260729
- Korean J Obstet Gynecol.
- 1997 Jan;40(1):198-202.
Osteogenesis imperfecta is a relatively rare genetic condition of breakable bones with an incidence of 1 per 20,000~60,000. The clinical, genetic, and biochemical heterogeneity in osteogenesis imperfecta allows to least... -
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- Ostogenesis Imperfecta: Report of 5 Cases
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Chung CY, Moon MS
- KMID: 2464356
- J Korean Orthop Assoc.
- 1970 Jun;5(2):59-63.
- doi: 10.4055/jkoa.1970.5.2.59
Five cases of osteogenesis imperfecta are reported, and the available literatures concerning to its clinical pictures and treatments are reviewed. -
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- A Case of Osteogenesis Imperfecta
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An KW, Jung CZ, Joo HS, Moon SW
- KMID: 1676460
- J Korean Pediatr Soc.
- 1986 Jan;29(1):84-87.
No abstract available. -
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- A Case of Osteogenesis Imperfecta
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Song SW, Jung HS, Kim KT, Lee JH
- KMID: 1676125
- J Korean Pediatr Soc.
- 1985 Jan;28(1):90-94.
No abstract available. -
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- Two Cases of Osteogenesis Imperfecta Congenita
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Lim SS, Lee BH, Kim YH, Joe MK
- KMID: 1682646
- J Korean Pediatr Soc.
- 1988 Aug;31(8):1085-1090.
No abstract available. -
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- Analysis on Surgical Treatment of Osteogenesis Imperfecta
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Lee SH, Chang JS, Lim HC, Kim CW
- KMID: 2446427
- J Korean Orthop Assoc.
- 1985 Feb;20(1):175-182.
- doi: 10.4055/jkoa.1985.20.1.175
Three children with osteogenesis imperfecta who were treated with fragmentation, realignment and intramedullary rod fixation (Sofield and Millar, 1959) have been followed up for considerable period. Repeated fractures in other... -
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- The Blue Sclera in Osteogenesis Imperfecta
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Kim SE, Lim KH, Ahn CS
- KMID: 2336654
- J Korean Ophthalmol Soc.
- 1998 Jan;39(1):204-208.
Osteogenesis imperfecta is relatively rare hereditary disease. It is characterized by frequent multiple bone fractures, spine scoliosis due to fragility of bone and is often associated with blue sclera, deafness... -
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- Osteogenesis Imperfecta (Correction of Anterior Tibial Bowing): A case report
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Seo JS, Ihn JC
- KMID: 2373929
- Yeungnam Univ J Med.
- 1987 Aug;4(1):157-163.
- doi: 10.12701/yujm.1987.4.1.157
Osteogenesis imperfecta has been categorized as a heritable disorder of connective tissue affecting both bone and soft tissues and is characterized by fragility of bone, blue sclera, and deafness, less... -
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- A Case of Osteogenesis Imperfecta Type II
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Lee CI, Kim YA, Kim JJ, Shin DH
- KMID: 1698974
- J Korean Pediatr Soc.
- 1984 Jan;27(1):93-97.
No abstract available. -
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- Osteogenesis imperfecta and combined orthodontics and orthognathic surgery: a case report on two siblings
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Kim DY, Baik U, Jeon JH
- KMID: 2471115
- J Korean Assoc Oral Maxillofac Surg.
- 2020 Feb;46(1):70-77.
- doi: 10.5125/jkaoms.2020.46.1.70
Osteogenesis imperfecta is a heterogeneous group of connective tissue diseases that is predominantly characterized by bone fragility and skeletal deformity. Two siblings with undiagnosed type I osteogenesis imperfecta underwent orthognathic... -
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- A Case of Osteogenesis Imperfecta: Diagnosis in Uterus by Ultrasonogram
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Seol HJ, Kim MJ, Kim MK, Park HJ, Shin JH, An HS, Choi WY
- KMID: 2272085
- Korean J Obstet Gynecol.
- 2003 Jun;46(6):1246-1249.
Osteogenesis imperfecta is a heterogeneous group of disorders that are characterized by connective tissue defects resulting in bone fragility, blue sclera, impaired hearing, defective dentition, and hyperlaxibility of the joints.... -
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- A case of Congenital Osteogenesis Imperfecta
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Lee SY, Kang YH, Oh SK, Park MS, Park HD, Cha DH
- KMID: 1676604
- J Korean Pediatr Soc.
- 1986 May;29(5):111-114.
No abstract available. -
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- Simultaneous Bilateral Patellar Tendon Ruptures Associated with Osteogenesis Imperfecta
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Kim WH, Ha SH, Lee HJ
- KMID: 2355509
- J Korean Orthop Assoc.
- 2016 Oct;51(5):432-436.
- doi: 10.4055/jkoa.2016.51.5.432
Bilateral patella tendon rupture is rare, particulary when associated with osteogenesis imperfecta. Brittleness of the bone in osteogenenesis imperfect patients may cause this rupture. We report on this rare case... -
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- A radiologic study about effects of multiple osteotomy and intramedullary nail fixation upon changes of diaphyseal thickness in osteogenesis imperfecta
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Lee SH, Kim CW, Moon JY, Hong JS
- KMID: 1691205
- J Korean Orthop Assoc.
- 1993 Dec;28(7):2479-2482.
No abstract available. -
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- A Case of Osteogenesis Imperfecta associated with Aortic Regurgitation
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Jeon SH, Kim WG, Kim JK, Kim JS, Ryu JC, Hong SK, Hyon MS, Hwang HK
- KMID: 2306309
- Korean J Med.
- 1999 Feb;56(2):209-214.
Osteogenesis imperfecta is one of the groups of hereditary disorders of connective tissue which includes the Ehlers-Danlos syndrome, the Marfan syndrome, pseudoxanthoma elasticum, and Hurler syndrome. While cardiovascular involvement is associated with... -
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- A Case of Perinatal Lethal Osteogeenesis Imperfecta
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Jang SL, Cho YS, Kim BW, Hong SR, Park JY, Park YJ, Lee JH
- KMID: 2071932
- Korean J Perinatol.
- 1997 Mar;8(1):55-59.
Osteogenesis imperfecta is a rare congenital disease. It is a heterogeneous group of inherited disorders characterized by multiple bone fracture, blue sclera, hearing loss, abnormalities of dentition and widespread connective... -
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- Osteogenesis Imperfecta: Case Report
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Kang CJ, Ha SH, Lee SH, Park KH
- KMID: 2445425
- J Korean Orthop Assoc.
- 1989 Oct;24(5):1497-1502.
- doi: 10.4055/jkoa.1989.24.5.1497
Osteogenesis imperfecta is a hereditary condition characterized by fragility of bone, deafness, blue sclera, laxity of joints and a tendency to improvement with age. Authors experienced osteogenesis imperfecta that develped... -
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- Intramedullary rod fixation for the osteogenesis imperfecta and congenital pseudarthrosis of the tibia
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Lee DY, Choi IH, Chung CY, Shim JS, Jeon DG, Seo JB
- KMID: 1947491
- J Korean Orthop Assoc.
- 1992 Feb;27(1):247-254.
No abstract available. -
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- A Case of Osteogenesis Imperfecta Type II Misdiagnosed as a Camptomelic Syndrome in Uterus
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Youn YE, Kim SB, Kim HJ
- KMID: 2280605
- Korean J Perinatol.
- 2007 Jun;18(2):177-181.
Osteogenesis imperfecta is a very rare heterogeneous disorder and its overall incidence is estimated at 1/25,000 births. It is characterized by bone fragility, loss of bone mass, blue sclera, impaired... -
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- Spinal anesthesia during cesarean section in a patient with severe osteogenesis imperfecta: A case report
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Hwang DK, Oh JI, Yoon HJ, Kim SM, Jee YS, Lee IH, Shin YC
- KMID: 2092259
- Korean J Anesthesiol.
- 2009 Nov;57(5):662-665.
- doi: 10.4097/kjae.2009.57.5.662
Obstetric anesthesia in a parturient with severe osteogenesis imperfecta is challenging in many aspects, particularly concerning maternal pathophysiological problems and the technical difficulties of anesthesia. Here, we report a case... -
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