Craniosynostosis - Recognition, clinical characteristics, and treatment

被引:142
作者
Kajdic, Nina [1 ,2 ]
Spazzapan, Peter [2 ]
Velnar, Tomaz [2 ]
机构
[1] Univ Ljubljana, Med Fac, Chair Surg, Ljubljana, Slovenia
[2] Univ Med Ctr Ljubljana, Dept Neurosurg, Zaloska 7, Ljubljana 1000, Slovenia
关键词
Craniosynostosis; development; classification; diagnosis; treatment; POSTOPERATIVE HELMET THERAPY; CRANIAL SUTURES; NONSYNDROMIC CRANIOSYNOSTOSIS; CORONAL CRANIOSYNOSTOSIS; SURGICAL-TREATMENT; COMPLICATIONS; SYNOSTOSIS; DIAGNOSIS; MORPHOGENESIS; POPULATION;
D O I
10.17305/bjbms.2017.2083
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Craniosynostosis is a developmental craniofacial anomaly, resulting in impairment of brain development and abnormally shaped skull. The main cause of craniosynostosis is premature closure of one or more cranial sutures. It usually occurs as an isolated condition, but may also be associated with other malformations as part of complex syndromes. When left untreated, craniosynostosis can cause serious complications, such as developmental delay, facial abnormality, sensory, respiratory and neurological dysfunction, anomalies affecting the eye, and psychological disturbances. Thus, early diagnosis, expert surgical techniques, postoperative care, and adequate follow-up are of vital importance in treating craniosynostosis.
引用
收藏
页码:110 / 116
页数:7
相关论文
共 61 条
[1]   The course of positional cranial deformation from 3 to 12 months of age and associated risk factors: a follow-up with 3D imaging [J].
Aarnivala, Henri ;
Vuollo, Ville ;
Harila, Virpi ;
Heikkinen, Tuomo ;
Pirttiniemi, Pertti ;
Holmstrom, Lasse ;
Valkama, A. Marita .
EUROPEAN JOURNAL OF PEDIATRICS, 2016, 175 (12) :1893-1903
[2]  
Accardi Manuela Chiara, 2009, J Prenat Med, V3, P31
[3]   A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003 [J].
Boulet, Sheree L. ;
Rasmussen, Sonja A. ;
Honein, Margaret A. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (08) :984-991
[4]   Craniosynostosis: Caring for Infants and Their Families [J].
Burokas, Laura .
CRITICAL CARE NURSE, 2013, 33 (04) :39-51
[5]   Craniosynostosis and maternal smoking [J].
Carmichael, Suzan L. ;
Ma, Chen ;
Rasmussen, Sonja A. ;
Honein, Margaret A. ;
Lammer, Edward J. ;
Shaw, Gary M. .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2008, 82 (02) :78-85
[6]   Recent advances in craniofacial morphogenesis [J].
Chai, Yang ;
Maxson, Robert E., Jr. .
DEVELOPMENTAL DYNAMICS, 2006, 235 (09) :2353-2375
[7]   Molecular signaling in pathogenesis of craniosynostosis: the role of fibroblast growth factor and transforming growth factor-β [J].
Chim, Harvey ;
Manjila, Sunil ;
Cohen, Alan R. ;
Gosain, Arun K. .
NEUROSURGICAL FOCUS, 2011, 31 (02)
[8]   Minimally Invasive Suturectomy and Postoperative Helmet Therapy : Advantages and Limitations [J].
Chong, Sangjoon ;
Wang, Kyu-Chang ;
Phi, Ji Hoon ;
Lee, Ji Yeoun ;
Kim, Seung-Ki .
JOURNAL OF KOREAN NEUROSURGICAL SOCIETY, 2016, 59 (03) :227-232
[9]  
Ciurea Alexandru Vlad, 2009, J Med Life, V2, P5
[10]   SUTURAL BIOLOGY AND THE CORRELATES OF CRANIOSYNOSTOSIS [J].
COHEN, MM .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 47 (05) :581-616