1)Styloid process syndrome茎突综合征
1.X-ray study of calcification of the ligaments in styloid process syndrome;茎突综合征患者茎突韧带钙化的X线摄片研究
2.Styloid Process Syndrome in 16 Cases of Misdiagnosis Analysis16例茎突综合征误诊原因分析
英文短句/例句
1.Treatment of styloid process syndrome with extraoral approach styloidectomy in 136 patients颈外径路茎突截短术治疗茎突综合征136例
2.Value of 64-slice spiral CT reconstruction technique in diagnosis of styloid process syndrome64排螺旋CT重建技术在茎突综合征中的诊断价值
3.Mutation Analysis on the Pathogenic Gene for Van Der Woude Syndrome范德伍兹综合征致病基因的突变检测
4.Study on Mutations of FBN1 and TGFBR2 Genes in Marfan Syndrome;马凡综合征FBN1和TGFBR2基因突变研究
5.Explorarat in Relations of Budd-Chiari Syndrome to FVLeiden and FⅡG20210A Mutations;布-加综合征与FVLeiden及FⅡG20210A突变关系的研究
6.Study on Mutations of FBN1, TGFBR2 and TGFBR1 Genes in Marfan Syndrome;马凡综合征FBN1、TGFBR2、TGFBR1基因突变研究
7.KCNJ5 Gly387Arg Mutation Responsible for Familial Long QT Syndrome;KCNJ5基因Gly387Arg突变导致家族性长QT综合征
8.Study on Genic Mutation in a Patient with Noonan SyndromeNoonan综合征1例基因突变研究
9.Analysis of MCP Mutations in 9 Chinese Children with Hemolytic Uremic Syndrome溶血尿毒综合征患儿MCP基因突变分析
10.Eya1 gene mutation test in a Goldenhar syndrome pedigreeGoldenhar综合征家系的eya1基因突变检测
11.Contrast Study of Conservative Treatments for Hypertrophia Symptom of the 5th Transverse Process of Lumbar Vertebra第5腰椎横突肥大综合征的保守疗法
12.Mutations of WNK kinases in patients with Gordon syndromeGordon综合征患者WNK基因突变研究
13.Cauda Equina Syndrome Resulting from Lumbar Disc herniation-A reporte of 12 cases腰椎间盘突出伴马尾神经综合征(附12例报告)
14.A Family with Brooke-Spiegler Syndrome: Analysis of the Clinical Features and Mutation Detection;Brooke-Spiegler综合征一家系的临床特点分析和突变检测
15.The Clinical Research on Acupotomology in Treatment of the Third Lumber Vertebrae Transverse Process Syndrome;小针刀治疗第三腰椎横突综合征临床疗效观察
16.Functional Expression of a Novel SCN5A Mutation K317N Identified in a Chinese Brugada Syndrome Family;中国人Brugada综合征基因突变K317N的功能表达研究
17.The Research on the Mutation of Coagulation Factor V of Diseased Tissues in Budd-Chiari Syndrome;布加氏综合征病变组织因子V突变的研究
18.Two Novel Mutations in Fibrillin-1 Gene from Patients with Marfan Syndrome;马凡综合征两种新的原纤蛋白-1基因突变
相关短句/例句
Stylohyoid syndrome茎突舌骨综合征
3)Small penis syndrome阴茎短小综合征
1.Small penis syndrome:Diagnosis and treatment;阴茎短小综合征的诊断与治疗
4)third lumbar vertebra TP syndrome腰椎横突综合征
5)No.3 vertebral transverse process syndrome腰三横突综合征
1.Methods:with GouPiGao to compare,the curative effect that carries out 4 weeks respectively for the 98 cases No.目的本试验通过临床疗效观察应用发热止痛贴与狗皮膏两种药物治疗腰三横突综合征,并进行了科学性、实用性的比较研究。
6)transverse syndrome of the third lumbar vertebrae第3腰椎横突综合征
1.Effect of acupotomy dissolution on pain threshold and ENK and β-EP in spinal cord and hypothalamus in rats with transverse syndrome of the third lumbar vertebrae;针刀松解法对第3腰椎横突综合征模型大鼠耐痛阈及脊髓与下丘脑ENK、β-EP的影响
延伸阅读
三倍体综合征和三倍体与二倍体混合体综合征三倍体综合征和三倍体与二倍体混合体综合征 三倍体指增加一组额外的染色体，约占妊娠的2%。额外的染色体多来自父亲，66%由于两次受精，24%由于所受的精子是二倍体，10%由于受精的卵是二倍体。胎儿大都流产，约为染色体异常自然流产的20%。孕妇可以伴发不同程度的妊高征，胎儿由于胎盘囊性变或细胞遗传学异常而死亡，只有3%的69，XXY存活。偶有三倍体婴儿在妊娠28周后出生，二倍体与三倍体混合体综合征更少见，均有严重的发育缺陷。表现：胎盘大有囊性变。骨骼方面混合体综合征者骨骼生长不对称。颅骨发育不良，后囟门大，眼距过宽，虹膜缺损，甚至小眼。鼻梁低，耳畸形，口颌小。第3、4指并指，通贯掌纹，马蹄内翻畸形足。先天性心脏病(心房和心室间隔缺损)。男性尿道下裂，阴茎小，隐睾，睾丸间质细胞增生。脑异常。肾上腺发育不全，肾畸形。此类综合征胎体大多流产，出生后也会早期死亡。存活的二倍体与三倍体混合体一般都有精神运动障碍。
