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Cleidocranial dysostosis. A review of 40 new cases.

作者信息

Jarvis J L, Keats T E

出版信息

Am J Roentgenol Radium Ther Nucl Med. 1974 May;121(1):5-16. doi: 10.2214/ajr.121.1.5.

DOI:10.2214/ajr.121.1.5
PMID:4833883
Abstract
摘要

相似文献

1
Cleidocranial dysostosis. A review of 40 new cases.锁骨颅骨发育不全。40例新病例综述。
Am J Roentgenol Radium Ther Nucl Med. 1974 May;121(1):5-16. doi: 10.2214/ajr.121.1.5.
2
[Cleidocranial dysostosis].[锁骨颅骨发育不全]
Chir Organi Mov. 1970;59(2):160-6.
3
Cleidocranial dysostosis.锁骨颅骨发育不全
Pediatr Emerg Care. 2013 Jul;29(7):867-9. doi: 10.1097/PEC.0b013e31829a90cf.
4
[Cleidocranial dysostosis. Contribution to its study apropos of 2 personal cases (an isolated and a familial form)].[锁骨颅骨发育不全。基于两例个人病例（一例散发和一例家族性病例）对其研究的贡献]
Rev Med Interne. 1984 Mar;5(1):76-82. doi: 10.1016/s0248-8663(84)80084-3.
5
Cleidocranial dysplasia.锁骨颅骨发育不全
Indian Pediatr. 1995 May;32(5):588-92.
6
[Pelvicocleidocranial dysostosis].
Fortschr Geb Rontgenstr Nuklearmed. 1970 Jul;113(1):49-59.
7
[Familial occurrence of cleidocranial dysostosis].[锁骨颅骨发育不全的家族性发病情况]
Cesk Radiol. 1972 Mar;26(2):92-6.
8
[Abortive sign of cleidocranial dysostosis--congenital pseudoarthrosis of the clavicle].[锁骨颅骨发育不全的顿挫征——先天性锁骨假关节]
Beitr Orthop Traumatol. 1968;15(11):645-8.
9
[Cleidocranial dysostosis: a clinicoradiologic study of 2 sisters].[锁骨颅骨发育不全：对两姐妹的临床放射学研究]
Radiol Med. 1980 Oct;66(10):713-5.
10
[Cleido-cranial dysplasia. Contribution to study of this disease on the basis of four cases (author's transl)].
Rev Stomatol Chir Maxillofac. 1978;79(1):35-51.

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Demographic, clinical, and radiological characteristics of cleidocranial dysplasia: A systematic review of cases reported in south America.锁骨颅骨发育不全的人口统计学、临床和放射学特征：对南美洲报告病例的系统评价
Ann Med Surg (Lond). 2022 Apr 10;77:103611. doi: 10.1016/j.amsu.2022.103611. eCollection 2022 May.
2
A Prosthodontic Approach as a Complementary Solution for a Complicated Orthodontic Treatment of a Patient with Cleidocranial Dysplasia.一种修复治疗方法作为锁骨颅骨发育不全患者复杂正畸治疗的补充解决方案。
Case Rep Dent. 2021 Jul 6;2021:6618813. doi: 10.1155/2021/6618813. eCollection 2021.
3
Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia.
一个家族性罕见常染色体显性遗传性 cleidocranial dysplasia 中 RUNX2 基因的新剪接位点突变的鉴定。
Iran Biomed J. 2021 Jul 1;25(4):297-302. doi: 10.52547/ibj.25.4.297.
4
Combined surgical-orthodontic treatment of patients with cleidocranial dysplasia: case report and review of the literature.联合外科-正畸治疗颅锁骨发育不全患者：病例报告及文献复习。
Orphanet J Rare Dis. 2018 Dec 4;13(1):217. doi: 10.1186/s13023-018-0959-3.
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Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review.通过全外显子组测序鉴定一个有多生牙和颅面发育异常家族中RUNX2基因的新突变：病例报告及文献复习
Medicine (Baltimore). 2018 Aug;97(32):e11328. doi: 10.1097/MD.0000000000011328.
6
Aesthetic Facial Correction of Cleidocranial Dysplasia.锁骨颅骨发育不全的面部美学矫正
Arch Craniofac Surg. 2016 Jun;17(2):82-85. doi: 10.7181/acfs.2016.17.2.82. Epub 2016 Jun 21.
7
Familial Cleidocranial Dysplasia.家族性锁骨颅骨发育不全
Int J Clin Pediatr Dent. 2010 Jan-Apr;3(1):57-61. doi: 10.5005/jp-journals-10005-1055. Epub 2010 Apr 15.
8
Histological examination and clinical evaluation of the jawbone of an adult patient with cleidocranial dysplasia: a case report.一名锁骨颅骨发育不全成年患者颌骨的组织学检查与临床评估：病例报告
Int J Clin Exp Pathol. 2015 Jul 1;8(7):8521-31. eCollection 2015.
9
Cleidocranial dysplasia syndrome: clinical characteristics and mutation study of a Chinese family.锁骨颅骨发育不全综合征：一个中国家系的临床特征及突变研究
Int J Clin Exp Med. 2013 Oct 25;6(10):900-7. eCollection 2013.
10
Cleidocranial dysplasia: complete clinical, radiological and histological profiles.锁骨颅骨发育不全：完整的临床、放射学和组织学特征
BMJ Case Rep. 2013 Mar 20;2013:bcr2013009015. doi: 10.1136/bcr-2013-009015.