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进行性纤维发育不良性骨化症研究进展 被引量:1

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摘要 进行性纤维发育不良性骨化症或称进行性骨化性纤维发育不良(fibrodysplasia ossificans progressiva,FOP),亦称作进行性肌肉骨化症或进行性骨化性肌炎(myositis ossificans progressiva,MOP),多发生于儿童,特征为筋膜、韧带、肌腱、关节囊及骨骼肌间隙中结缔组织进行性骨化,合并特殊骨骼畸形(主要是拇趾短大、外翻)导致关节活动受限、功能丧失。近些年来人们对该病深入研究,取得了一些新进展。
出处 《中国骨肿瘤骨病》 CAS 2007年第1期44-47,共4页 Chinse Journal Of Bone Tumor And Bone Disease
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参考文献27

  • 1[1]Kaplan FS,Glaser DL,Shore EM.Fibrodysplasia (myositis) ossificans progressiva.In Favus MJ (ed).Primer on the metabolic bone diseases and disorders of mineral metabolism.Fifth Edition.The American Society for Bone and Mineral Research,Lippincott-Raven,Philadelphia,2003.
  • 2[2]Kaplan FS,Shore EM,Connor JM.Fibrodysplasia ossificans progressiva (FOP).In Royce PM,Steinmann B (eds).Connective tissue and its heritable disorders.New York,Wiley-Liss,Inc,2002:827-840.
  • 3[3]Patin G.Lettres choisis de feu M.Guy Patin.Letter of August 27,1648,to AF.Cologne P.du Laurens,1692.Tome 1,vol.5,p.28.
  • 4[4]Kaplan FS,Fiori J,DE LA Pena LS,et al.Dysregulation of the BMP-4 signaling pathway in fibrodysplasia ossificans progressiva.Ann N Y Acad Sci.2006,1068:54-65.
  • 5[5]Shore EM,Xu M,Feldman GJ,et al.A recurrent mutation in the BMP type Ⅰ receptor ACVR 1 causes inherited and sporadic fibrodysplasia ossificans progressiva.Nat Genet,2006,38:525-527.
  • 6[6]Ahn J,Serrano de la Pena L,Shore EM,et al.Paresis of a bone morphogenetic protein-antagonist response in a genetic disorder of heterotopic skeletogenesis.J Bone Joint Surg Am,2003,85-A:667-674.
  • 7[7]Semonin O,Fontaine K,Daviaud C,et al.Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva.Am J Med Genet,2001,102:314-317.
  • 8[8]Fiori JL,Billings PC,de la Pena LS,et al.Dysregulation of the BMP-p38 MAPK signaling pathway in cells from patients with fibrodysplasia ossificans progressiva (FOP).J Bone Miner Res,2006 Jun;21(6):902-909.
  • 9[9]Kan L,Hu M,Gomes WA,et al.Transgenic mice overexpressing BMP4 develop a fibrodysplasia ossificans progressiva (FOP)-like phenotype.Am J Pathol,2004,165:1107-1115.
  • 10[10]Glaser DL,Economides AN,Wang L,et al.In vivo somatic cell gene transfer of an engineered noggin mutein prevents BMP4-induced heterotopic ossification.J Bone Joint Surg Am,2003,12:2332-2342.

同被引文献13

  • 1童杰,邓展生,周江南,龙文荣,王锡阳,孙太存,鞠洪斌.进行性骨化性肌炎1例报告并文献复习[J].中国现代医学杂志,2005,15(17):2718-2720. 被引量:5
  • 2Kitterman JA,Kantanie S,Rocke DM,et al.Iatmgenic harmc caused by diagnostic errors in fibrodysplasia ossificans progressiva[J].Pediatric,2005,116(5):e654-e661.
  • 3Connor JM,Evans DA.Fibrodysplasia ossificans progressiva.The clinical features and natural hisory of 34 patients[J].J Bone Joint Surg Br,1982,64(1):76-83.
  • 4Tulchinsky M.Diagnostic features of fibrodysplasia(myositis) ossificans pmgressive on bone scan[J].Clin Nucl Med,2007,32(8):616-619.
  • 5Kan L,Hu M,Gomes WA,et al.Transgenic mice overex-pressing BMP4 develop a fibrodysplasia ossificans progressiva(FOP)-like phenotype[J].Am J Pathol,2004,165(4):1107-1115.
  • 6Kaplan FS,Xu M,Glaser D L.Early diagnosis of fibrodysplasia ossificans progressive[J].Pediatrics,2008,l21(5):e1295-el300.
  • 7Kaplan FS,Xu M,Seemann P,et al.Classic and atypical fibrodysplasia ossificans progressiva(FOP) phenotypes are caused by mutations in the bone morphogenetic protein(BMP) type 1 receptor ACVR1[J].Human Mutation,2009,30(3):379-390.
  • 8Hagiwara H,Aida N,Machida J,et al.Contrast-enhanced MRI of an early preosseous lession of fibrodysplasia ossificans progressiva in a 21-month-old boy[J].Am J Roentgenol,2003,181(4):1145-1147.
  • 9Mahboubi S,Glaser DL,Shore EM,et al.Fibrodysplasia ossificans progressiva[J].Pediatr Radiol,2001,31(5):307-314.
  • 10Shih WJ,Hackett MT,Stipp V,et al.Myositis ossificans demonstrated by positive gallium-67 and technetium-99m HMDP bone imaging but negative technetium-99m-MIBI imaging[J].J Nucl Med Technol,1999,27(1):48-50.

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