Crouzon Syndrome Associated with Congenital Coarctation of Aorta.
作者信息
Meng Bing, Zhang Hui
机构信息
Department of Cardiac Surgery, Children's Hospital Affiliated to the Capital Institute of Pediatrics, Beijing 100020, China.
出版信息
Chin Med J (Engl). 2018 Jun 20;131(12):1498-1499. doi: 10.4103/0366-6999.233963.
Abstract
摘要
相似文献
1
Crouzon Syndrome Associated with Congenital Coarctation of Aorta.克鲁宗综合征合并先天性主动脉缩窄
Chin Med J (Engl). 2018 Jun 20;131(12):1498-1499. doi: 10.4103/0366-6999.233963.
2
[Problems of associated defects in aortic coarctation].
Thoraxchir Vask Chir. 1971 Oct;19(5):415-8. doi: 10.1055/s-0028-1099159.
3
[On the association of aortic isthmus stenosis with other cardiovascular anomalies].
Radiol Diagn (Berl). 1968;9(2):174-5.
4
Unusual combination of congenital heart lesions in a child with Noonan's syndrome.努南综合征患儿先天性心脏病变的不寻常组合。
Pediatr Cardiol. 1982;3(1):23-6. doi: 10.1007/BF02082326.
5
[Coarctation of the aortic isthmus (neonatal emergencies excepted)].
Rev Med Liege. 1995 Jul;50(7):298-304.
6
[Left-side aortic arch and right-side aorta descendens, associated with aortic coarctation].[左侧主动脉弓与右侧降主动脉，伴主动脉缩窄]
Orv Hetil. 1977 Sep 4;118(36):2155-58.
7
Coarctation of the aorta in Kabuki syndrome.歌舞伎综合征中的主动脉缩窄
Arch Dis Child. 1994 Jun;70(6):512-4. doi: 10.1136/adc.70.6.512.
8
The liver in congenital heart disease. Effects of infantile coarctation of the aorta and the hypoplastic left heart syndrome in infancy.
Am J Dis Child. 1970 May;119(5):390-4.
9
Repair of coarctation of the thoracic aorta by patch graft aortoplasty.
J Thorac Cardiovasc Surg. 1974 Nov;68(5):696-704.
引用本文的文献
1
Extremely severe scoliosis, heterotopic ossification, and osteoarthritis in a three-generation family with Crouzon syndrome carrying a mutant c.799T>C FGFR2.三代家系中伴有 FGFR2 c.799T>C 突变的 Crouzon 综合征患者出现严重脊柱侧凸、异位骨化和骨关节炎
Mol Genet Genomic Med. 2019 Sep;7(9):e843. doi: 10.1002/mgg3.843. Epub 2019 Jul 18.
本文引用的文献
1
Ventricular septal defect in Crouzon Syndrome: case report.克鲁宗综合征合并室间隔缺损：病例报告
Genet Couns. 2012;23(4):519-22.
2
Recognizing craniosynostosis.认识颅缝早闭。
Neonatal Netw. 2009 Nov-Dec;28(6):369-76. doi: 10.1891/0730-0832.28.6.369.
3
Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene.一名患有克鲁宗综合征且成纤维细胞生长因子受体（FGFR）-2基因发生突变的患者出现心内膜垫缺损。
Clin Genet. 2007 Oct;72(4):305-7. doi: 10.1111/j.1399-0004.2007.00861.x.
4
A model for the pharmacological treatment of crouzon syndrome.一种用于治疗克鲁宗综合征的药物治疗模型。
Neurosurgery. 2006 Jul;59(1):210-5; discussion 210-5. doi: 10.1227/01.NEU.0000224323.53866.1E.
5
[Coexistence of Crouzon syndrome with ventricular septal defect].[克鲁宗综合征与室间隔缺损共存]
Wiad Lek. 2003;56(5-6):298-9.
6
Crouzon syndrome: association with absent pulmonary valve syndrome and severe tracheobronchomalacia.克鲁宗综合征：与肺动脉瓣缺如综合征及严重气管支气管软化症的关联。
Pediatr Pulmonol. 2002 Dec;34(6):478-81. doi: 10.1002/ppul.10176.
7
Differential expression of fibroblast growth factor receptors in human digital development suggests common pathogenesis in complex acrosyndactyly and craniosynostosis.成纤维细胞生长因子受体在人类手指发育中的差异表达表明复杂并指畸形和颅缝早闭存在共同的发病机制。
Plast Reconstr Surg. 2001 May;107(6):1331-8; discussion 1339-45. doi: 10.1097/00006534-200105000-00001.
Zotero 插件