1) Dandy-Walker syndrome
Dandy-Walker综合征
1.
Clinical characteristics of 6 cases of Dandy-Walker syndrome
Dandy-Walker综合征临床分析
2.
Objective To evaluate the third plane image of the three-dimensional sonography(3D US) for the quantitative analysis of the cerebellar vermis in normal and Dandy-Walker syndrome(DWS) fetuses.
目的探讨产前三维超声第三平面成像方法定量分析Dandy-Walker综合征胎儿小脑蚓部发育的辅助诊断价值。
3.
Objective To explore the diagnostic value of prenatal ultrasound in fetal Dandy-Walker syndrome.
目的探讨Dandy-Walker综合征的产前超声诊断价值。
2) Dandy-Walker malformation
Dandy-Walker畸形
1.
Ultrasonic diagonosis of Dandy-Walker malformation in prenatal: case report;
产前超声诊断Dandy-Walker畸形1例
2.
Prenatal sonographic diagnosis of fetal Dandy-Walker malformation;
胎儿Dandy-Walker畸形的产前超声诊断
3.
Objective To explore the diagnostic value of prenatal ultrasound in fetal Dandy-Walker malformation.
目的探讨产前超声检查对胎儿Dandy-Walker畸形的诊断价值。
3) POEMS syndrome
POEMS综合征
1.
Clinical Analysis of 5 Cases of POEMS Syndrome;
POEMS综合征5例临床分析
2.
Clinical manifestations and diagnosis of POEMS syndrome;
POEMS综合征的临床表现及诊断
3.
Clinical analysis of misdiagnosis of patients with POEMS syndrome;
POEMS综合征临床误诊原因分析
4) Turner syndrome
Turner综合征
1.
Karyotypes and pelvic ultrasonography in children with Turner syndrome;
Turner综合征患儿染色体核型和盆腔超声的分析
2.
Effects of recombinant human growth hormone on height in Turner syndrome.;
生长激素对Turner综合征的促身高作用
3.
Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization;
Turner综合征患儿标记染色体的来源研究
5) Tourette's syndrome
Tourette综合征
1.
Study on the character of auditory P300 of Tourette's syndrome with or without behavioral problems;
Tourette综合征伴或不伴行为问题的P300研究
6) Mirizzi syndrome
Mirizzi综合征
1.
The clinical analysis of diagnosis and laparoscopic treatment 37cases with Mirizzi syndrome;
Mirizzi综合征的诊断及腹腔镜治疗的临床分析(附37例报告)
2.
Diagnosis and treatment of 53 patients with Mirizzi syndrome;
Mirizzi综合征诊治分析53例
3.
Diagnosis and treatment of 14 patients with Mirizzi syndrome;
Mirizzi综合征诊治14例
补充资料：3X综合征
3X综合征
XXX syndrome
本病又称为超雌。其核型为47，XXX，比正常女性多了一条X染色体。主要是由于母亲形成卵子时，X染色体不分离，形成24，XX的种子，与正常X型精子受精形成。其外貌为女性，常有内眦赘皮、眼距宽，多数患者性腺正常，月经与性发育正常、可受孕。但性发育也可幼稚，或有原发闭经。多伴智力障碍。有些病例核型为XX/47，XXX的嵌合体。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条