CONGENITAL相关论文
目的:探讨天津市婴儿发育性髋关节发育不良（developmental dysplasia of the hip，DDH）的B超筛查Graf分型结果及危险因素。方法:回顾性......
目的:通过对心脏出生缺陷（CBD）胎儿进行准确产前诊断、分级咨询后，结合胎儿CBD分级对其临床随访结果进行研究，为产前-产后一体化治疗提......
目的:评价经食管超声测量肺静脉血流频谱评估复杂先天性心脏病患儿术中左心房压力(LAP)的可行性。方法:全麻下行手术治疗且术中需......
先天性桡尺骨近端融合（congenital proximal radioulnar synostosis，PRUS）是一种较为常见的儿童上肢先天性畸形，常见于男性患儿。目前......
先天性左心室室壁瘤（CLVA）是临床上一种十分罕见的心脏畸形，临床表现不典型，超声心动图及心脏磁共振成像检查是诊断 CLVA的重要方法。C......
先天性左心室室壁瘤（CLVA）少见，而多发性CLVA则属临床罕见，容易误诊。本文报告一例以“阵发性室性心动过速”为首发表现的多发性CLVA，开......
Objective:Thisstudyinvestigatesthelongtermresultsofcongenitalclubfoottreatedwithonestagesurgicalprocedure:tibialisanteri......
Comparison of posterior release, internal traction, final osteotomy and fusion with one-stage poster
Introduction To compare efficacy, safety, and costs of posterior release, internal distraction, and final spinal fusion ......
Objective To explore the clinical value of dual-source CT in diagnosis of congenital heart diseases.Methods 68 cases of ......
目的:探讨磷脂酰肌醇蛋白聚糖3（glypican-3，n GPC3）基因变异致Simpson-Golabi- Behmel 综合征（Simpson-Golabi-Behmel syndrome，SG......
Predicting Perinatal Outcomes in Fetuses with Congenital Diaphragmatic Hernia Using Ultrasound and M
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Correction of Congenital Symmastia with Macromastia: Report of a Rare Case and Devised Treatment Alg
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目的分析复杂型先天性心脏病（CCHD）患儿的临床诊疗现状及术后死亡的影响因素，优化CCHD的围术期管理，为临床决策提供新的科学依据。方法......
目的提出儿童股骨近端前倾程度的一种新的测量指标，即股骨颈-小转子前倾角（femoral neck-lesser trochanter anteversion，FN-LTA），并探......
目的探讨多学科联合诊疗在先天性束带综合征中的意义。方法回顾性分析中国人民解放军空军军医大学第一附属医院2017年1月至2020年1......
Predicting Perinatal Outcomes in Fetuses with Congenital Diaphragmatic Hernia Using Ultrasound and M
Congenital diaphragmatic hernia is a congenital fetal disease, which mainly causes pulmonary hypoplasia and pulmonary hy......
<strong>Introduction:</strong><span style=“white-space:normal;”><span style=“font-family:;” “=”\"> Congenitally ......
Morphological Characteristics of the Artery of the Atrioventricular Node by Congenital Heart Defects
The objective of the work is to study the topographic and anatomical characteristics of the atrioventricular node’s art......
<strong>Introduction:</strong><span><span><span style=“font-family:;” “=”\"><span> Bart’s syndrome is a rare neon......
<strong>Background:</strong> Malaria in pregnancy poses a great health risk to the mother and her fetus and causes abort......
目的:探讨n 18F-脱氧葡萄糖(FDG)PET在评估先天性心脏病相关肺动脉高压(PAH-CHD)患者的肺组织葡萄糖摄取速率及其与肺动脉血......
先天性裂手是一类较为罕见的先天性手部畸形。裂手畸形的特征是中央指列缺损，相邻边缘指间变窄或并指，在手部中央形成裂隙。手术适应......
BACKGROUND Retrocorneal hyaline scrolls are a rare phenomenon.We report a case of bilateral retrocorneal hyaline scrolls......
Turner syndrome with positive SRY gene and non-classical congenital adrenal hyperplasia: A case repo
BACKGROUND Co-morbidity of SRY gene turner syndrome(TS)with positive SRY gene and nonclassical congenital adrenal hyperp......
Prenatal diagnosis of cor triatriatum sinister associated with early pericardial effusion:A case rep
BACKGROUND Cor triatriatum sinistrum or cor triatriatum sinister is a rare congenital heart disease that accounts for ap......
BACKGROUND Double outlet right ventricle(DORV)is a rare and complex congenital heart defect,and the surgical repairs var......
BACKGROUND CYP21A2 gene mutations may all cause reduction or loss of 21-hydroxylase activity,leading to development of c......
Syringocystadenoma papilliferum(SCAP)is a rare benign skin tumor that develops from the apocrine or eccrine glands.Here,......
Prenatal diagnosis of triphalangeal thumb-polysyndactyly syndrome by ultrasonography combined with g
BACKGROUND Triphalangeal thumb-polysyndactyly syndrome(TPT-PS)is a rare type of congenital limb deformity,and most studi......
BACKGROUND Congenital factor VII deficiency(FVIID)is a rare autosomal recessive genetic disorder.The clinical manifestat......
BACKGROUND Pediatric temporal fistulae are rarely reported in the literature.Dissemination of these cases can help infor......
<strong>Introduction:</strong><b><span style=“font-family:;” “=”“> </span></b><span style=”font-family:Verdana;\......
Alpha-dystroglycanopathy(α-DGP)is a subtype of congenital muscular dystrophies(CMDs)with autosomal recessive inheritanc......
BACKGROUND The ATP6AP1 gene coding for the accessory protein Ac45 of the vacuolar-type adenosine triphosphatases(V-ATPas......
Homozygous deletion, c. 1114-1116del, in exon 8 of the CRPPA gene causes congenital muscular dystrop
BACKGROUND Congenital muscular dystrophy(CMD)is a clinically and genetically heterogeneous group of inherited muscle dis......
As an indispensable part of congenital cataract surgery,intraocular lens(IOL)implantation in infantile patients has long......
Development in medical intervention has significantly decreased the mortality rates for children with complex congenit......
AIM:To review the demographics,clinical manifestations,and surgical experiences of patients with congenital ocular count......
BACKGROUND Children with congenital glaucoma are often accompanied by acquired epiblepharon in the lower eyelid,which ca......
Current Advances in Transcatheter Intervention for Children Born with Congenital Heart Defects: A Re
This review aims to sum up the improvements witnessed in the field of interventional cardiology during recent times. The......
目的探讨影响先天性膈疝（congenital diaphragmatic hernia，CDH）胎儿生存的因素，并建立CDH的预测模型。方法对2010年1月1日至2018年12......
