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The first and second branchial arch syndrome.

作者信息

Grabb W C

出版信息

Plast Reconstr Surg. 1965 Nov;36(5):485-508. doi: 10.1097/00006534-196511000-00001.

DOI:10.1097/00006534-196511000-00001
PMID:5320180
Abstract
摘要

相似文献

1
The first and second branchial arch syndrome.第一、二鳃弓综合征
Plast Reconstr Surg. 1965 Nov;36(5):485-508. doi: 10.1097/00006534-196511000-00001.
2
[Congenital malformations in the area of the derivatives of the branchial arch].[鳃弓衍生物区域的先天性畸形]
Minerva Chir. 1960 Mar 15;15:243-9.
3
On hemifacial microsomia. The first and second branchial arch syndrome.关于半侧颜面短小畸形。第一、二鳃弓综合征。
Plast Reconstr Surg. 1973 Mar;51(3):268-79.
4
[2 cases of so-called "first and second branchial arch syndrome" with unilateral paralysis of the face].2例所谓“第一、二鳃弓综合征”伴单侧面部麻痹
Jibiinkoka. 1970 Sep;42(9):669-72.
5
Pathogenesis of dysplasias of the face and the ear and dystopias of the temporal region.面部发育异常、耳部发育异常及颞区异位的发病机制。
Int J Pediatr Otorhinolaryngol. 1984 May;7(2):159-72. doi: 10.1016/s0165-5876(84)80040-3.
6
Setleis bitemporal "forceps marks" syndrome and its pathogenesis: a case report.
Acta Paediatr Jpn. 1991 Apr;33(2):186-90. doi: 10.1111/j.1442-200x.1991.tb01541.x.
7
Variability versus "incidental findings" in the first and second branchial arch syndrome: unilateral variants with anophthalmia.
Birth Defects Orig Artic Ser. 1971 Jun;7(7):103-8.
8
Branchial arch malformations in infants of diabetic mothers: two case reports and a review.糖尿病母亲所生婴儿的鳃弓畸形:两例病例报告及文献综述
Am J Med Genet. 1982 Oct;13(2):125-30. doi: 10.1002/ajmg.1320130204.
9
Branchio-oculo-facial syndrome: broadening the spectrum.鳃-眼-面综合征:拓宽疾病谱
Am J Med Genet. 1994 Feb 15;49(4):414-21. doi: 10.1002/ajmg.1320490413.
10
[A typical case of Smith-Lemli-Opitz syndrome: nosologic problems and overlapping syndromes].[史密斯-勒米-奥皮茨综合征典型病例:疾病分类问题与重叠综合征]
Pathologica. 1990 Sep-Oct;82(1081):539-42.

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Assessment and Identification of Improvement Areas for Facial Symmetry in Hemifacial Microsomia (Type IIB) Using Three-dimensional Measurements.使用三维测量评估和识别半侧颜面短小畸形(IIB型)面部对称性的改善区域
Plast Reconstr Surg Glob Open. 2024 Jun 10;12(6):e5877. doi: 10.1097/GOX.0000000000005877. eCollection 2024 Jun.
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Three-dimensional Hemifacial Microsomia Classification with New Subtypes Based on the Pruzansky and Kaban Classification.基于普鲁赞斯基和卡班分类法的具有新亚型的三维半侧颜面短小畸形分类
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Growth characteristics and classification systems of hemifacial microsomia: a literature review.
半侧颜面短小畸形的生长特征及分类系统:文献综述
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Loeys-Dietz syndrome and Goldenhar syndrome unveiled together.洛伊迪茨综合征和金哈综合征同时显现。
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Interrater Reliability for Classifying Craniofacial Microsomia Severity: A Call for Objective Evaluation.颅面微小畸形严重程度分类的评分者间信度:呼吁进行客观评估。
Cleft Palate Craniofac J. 2025 Apr;62(4):619-626. doi: 10.1177/10556656231216557. Epub 2023 Nov 22.
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Characterizing Speech Phenotype in Individuals With Craniofacial Microsomia: A Scoping Review.探讨颅面短小畸形患者的言语表现特征:范围综述。
Am J Speech Lang Pathol. 2024 Jan 3;33(1):485-504. doi: 10.1044/2023_AJSLP-23-00152. Epub 2023 Nov 6.
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Orthognathic surgery with iliac bone grafting for an interpositional gap in a patient with type III hemifacial microsomia: A case report.采用髂骨移植的正颌外科手术治疗Ⅲ型半侧颜面短小畸形患者的间隙植入:一例报告。
JPRAS Open. 2023 Jun 12;37:55-62. doi: 10.1016/j.jpra.2023.06.001. eCollection 2023 Sep.
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Benefits of bone conduction hearing aid in children with unilateral aural atresia.骨导助听器对单侧先天性外中耳畸形儿童的益处。
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Knockout in Zebrafish Causes Abnormal Craniofacial Chondrogenesis by Regulating FGF Pathway.斑马鱼基因敲除通过调控 FGF 通路引起颅面部软骨生成异常。
Genes (Basel). 2023 Mar 30;14(4):838. doi: 10.3390/genes14040838.
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Characterising the speech phenotype in individuals with craniofacial microsomia: a scoping review protocol.探讨颅面短小畸形患者的言语表型:系统评价方案
BMJ Open. 2023 Feb 28;13(2):e069233. doi: 10.1136/bmjopen-2022-069233.