Syndromes of the First and Second Branchial Arches, Part 2: Syndromes

被引:26
作者
Johnson, J. M. [1 ]
Moonis, G. [2 ]
Green, G. E. [3 ]
Carmody, R. [4 ]
Burbank, H. N. [1 ]
机构
[1] Fletcher Allen Hlth Care, Dept Radiol, Div Neuroradiol, Burlington, VT 05401 USA
[2] Harvard Univ, Sch Med, Dept Radiol, Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[3] Univ Michigan, Dept Pediat Otolaryngol, Ann Arbor, MI 48109 USA
[4] Univ Arizona, Dept Radiol, Div Neuroradiol, Tucson, AZ 85724 USA
关键词
TREACHER-COLLINS-SYNDROME; AURICULO-CONDYLAR SYNDROME; 22Q11.2 DELETION SYNDROME; PIERRE-ROBIN-SEQUENCE; QUESTION MARK EAR; HEMIFACIAL MICROSOMIA; STICKLER-SYNDROME; CLEFT-PALATE; ANOMALIES; DIAGNOSIS;
D O I
10.3174/ajnr.A2073
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A variety of congenital syndromes affecting the face occur due to defects involving the first and second BAs. Radiographic evaluation of craniofacial deformities is necessary to define aberrant anatomy, plan surgical procedures, and evaluate the effects of craniofacial growth and surgical reconstructions. High-resolution CT has proved vital in determining the nature and extent of these syndromes. The radiologic evaluation of syndromes of the first and second BA should begin first by studying a series of isolated defects (cleft lip with or without CP, micrognathia, and EAC atresia) that compose the major features of these syndromes and allow a more specific diagnosis. After discussion of these defects and the associated embryology, we discuss PRS, HFM, ACS, TCS, Stickler syndrome, and VCFS.
引用
收藏
页码:230 / 237
页数:8
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