Implant therapy for a patient with osteogenesis imperfecta type I: review of literature with a case report

被引:4
作者
Prabhu, Shamit S. [1 ,4 ]
Fortier, Kevin [2 ]
May, Michael C. [3 ]
Reebye, Uday N. [4 ]
机构
[1] Wake Forest Sch Med, Winston Salem, NC 27101 USA
[2] Boston Univ, Henry M Goldman Sch Dent Med, Boston, MA 02215 USA
[3] Virginia Commonwealth Univ, Sch Dent, Richmond, VA 23284 USA
[4] Triangle Implant Ctr, 5318 NC Highway 55,Suite 106, Durham, NC 27713 USA
关键词
Osteogenesis imperfecta type I; Implant therapy; Brittle bone disease; DENTAL IMPLANTS; MUTATIONS; FORM; OSSEOINTEGRATION; REHABILITATION; IDENTIFICATION; AUGMENTATION; DEFICIENCY; DISORDERS; PLACEMENT;
D O I
10.1186/s40729-018-0148-0
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Bone fragility and skeletal irregularities are the characteristic features of osteogenesis imperfecta (OI). Many patients with OI have weakened maxillary and mandibular bone, leading to poor oral hygiene and subsequent loss of teeth. Improvements in implant therapy have allowed for OI patients to achieve dental restoration. However, there is limited available literature on implant therapy for patients with OI. The greatest challenge in the restoration process for OI patients in an outpatient setting is ensuring primary stability and osseointegration. Improvements in synthetic grafts improve successful implant placement and prevent predisposing patients to unnecessary procedures. This report details the successful restoration process of an OI type I patient's maxillary arch in addition to a review of the currently available literature.
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页数:8
相关论文
共 42 条
[1]   Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta [J].
Alanay, Yasemin ;
Avaygan, Hrispima ;
Camacho, Natalia ;
Utine, G. Eda ;
Boduroglu, Koray ;
Aktas, Dilek ;
Alikasifoglu, Mehmet ;
Tuncbilek, Ergul ;
Orhan, Diclehan ;
Bakar, Filiz Tiker ;
Zabel, Bernard ;
Superti-Furga, Andrea ;
Bruckner-Tuderman, Leena ;
Curry, Cindy J. R. ;
Pyott, Shawna ;
Byers, Peter H. ;
Eyre, David R. ;
Baldridge, Dustin ;
Lee, Brendan ;
Merrill, Amy E. ;
Davis, Elaine C. ;
Cohn, Daniel H. ;
Akarsu, Nurten ;
Krakow, Deborah .
AMERICAN JOURNAL OF HUMAN GENETICS, 2010, 86 (04) :551-559
[2]  
[Anonymous], 2016, Pediatr Dent, V38, P302
[3]   The genetic basis of inherited anomalies of the teeth. Part 2: Syndromes with significant dental involvement [J].
Bailleul-Forestier, Isabelle ;
Berdal, Ariane ;
Vinckier, Frans ;
de Ravel, Thomy ;
Fryns, Jean Pierre ;
Verloes, Alain .
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2008, 51 (05) :383-408
[4]   Brief report: Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta [J].
Barnes, Aileen M. ;
Cliang, Weizhong ;
Morello, Roy ;
Cabral, Wayne A. ;
Weis, MaryAnn ;
Eyre, David R. ;
Leikin, Sergey ;
Makareeva, Elena ;
Kuznetsova, Natalia ;
Uveges, Thomas E. ;
Ashok, Aarthi ;
Flor, Armando W. ;
Mulvihill, John J. ;
Wilson, Patrick L. ;
Sundaram, Usha T. ;
Lee, Brendan ;
Marini, Joan C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (26) :2757-2764
[5]   Dentofacial rehabilitation by osteodistraction, augmentation and implantation despite osteogenesis imperfecta [J].
Binger, T. ;
Ruecker, M. ;
Spitzer, W. J. .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2006, 35 (06) :559-562
[6]   Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial [J].
Bishop, Nick ;
Adami, Silvano ;
Ahmed, S. Faisal ;
Anton, Jordi ;
Arundel, Paul ;
Burren, Christine P. ;
Devogelaer, Jean-Pierre ;
Hangartner, Thomas ;
Eva Hosszu ;
Lane, Joseph M. ;
Lorenc, Roman ;
Makitie, Outi ;
Munns, Craig F. ;
Paredes, Ana ;
Pavlov, Helene ;
Plotkin, Horacio ;
Raggio, Cathleen L. ;
Loreto Reyes, Maria ;
Schoenau, Eckhard ;
Semler, Oliver ;
Sillence, David O. ;
Steiner, Robert D. .
LANCET, 2013, 382 (9902) :1424-1432
[7]   OSSEOINTEGRATION AND ITS EXPERIMENTAL BACKGROUND [J].
BRANEMARK, PI .
JOURNAL OF PROSTHETIC DENTISTRY, 1983, 50 (03) :399-410
[8]   BRITTLE BONES - FRAGILE MOLECULES - DISORDERS OF COLLAGEN GENE STRUCTURE AND EXPRESSION [J].
BYERS, PH .
TRENDS IN GENETICS, 1990, 6 (09) :293-300
[9]   Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta [J].
Cabral, Wayne A. ;
Chang, Weizhong ;
Barnes, Aileen M. ;
Weis, MaryAnn ;
Scott, Melissa A. ;
Leikin, Sergey ;
Makareeva, Elena ;
Kuznetsova, Natalia V. ;
Rosenbaum, Kenneth N. ;
Tifft, Cynthia J. ;
Bulas, Dorothy I. ;
Kozma, Chahira ;
Smith, Peter A. ;
Eyre, David R. ;
Marini, Joan C. .
NATURE GENETICS, 2007, 39 (03) :359-365
[10]   A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis Imperfecta Type V [J].
Cho, Tae-Joon ;
Lee, Kyung-Eun ;
Lee, Sook-Kyung ;
Song, Su Jeong ;
Kim, Kyung Jin ;
Jeon, Daehyun ;
Lee, Gene ;
Kim, Ha-Neui ;
Lee, Hye Ran ;
Eom, Hye-Hyun ;
Lee, Zang Hee ;
Kim, Ok-Hwa ;
Park, Woong-Yang ;
Park, Sung Sup ;
Ikegawa, Shiro ;
Yoo, Won Joon ;
Choi, In Ho ;
Kim, Jung-Wook .
AMERICAN JOURNAL OF HUMAN GENETICS, 2012, 91 (02) :343-348