Results 251 to 260 of about 423,772 (336)

Postnatal outcomes of referred cases with abnormal ultrasound findings of fetal gall bladder and cyst in the fetal liver. [PDF]

Obstet Gynecol Sci
Choi SR, Won HS, Chung JH, Lee MY, Koh J, Lee YJ.   +5 more
europepmc   +1 more source

Predictors of Adverse Perinatal Outcome in Twin Anemia Polycythemia Sequence: Evidence From a Single Center Cohort Study

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the perinatal outcome of monochorionic pregnancies complicated by Twin Anemia‐Polycythemia Sequence (TAPS) and identify prognostic factors associated with adverse outcomes. Methods A retrospective study (2012–2024) analyzed TAPS cases at a tertiary center.
Keren Zloto, Noa Rosenthal, Stav Cohen, Hagai Avnet, Boaz Weisz, Yoav Yinon   +5 more
wiley   +1 more source

Prenatal diagnosis of balanced translocation from three families: Six case reports. [PDF]

World J Clin Cases
Kan X, Xie YX, Yao L, Wang LY, Xia YX, Sun JQ, Bian ML, Yu L, Lu YL.   +8 more
europepmc   +1 more source

Fetal Pancreas in Growth Restriction: A Prenatal Window Into Metabolic and Genetic Risk

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Animal models have demonstrated impaired pancreatic islet development in fetal growth restriction (FGR) cases, which can become apparent at or before birth and persist into adulthood, resulting in glucose intolerance. This study assessed the relationship between fetal pancreatic biometry and FGR.
Hadas Miremberg, Catharina Bobrow, Noa Feldman, Noa Haggiag, Catherine Garel, Gustavo Malinger, Karina Krajden Haratz, Sharon Perlman   +7 more
wiley   +1 more source

Integration of molecular diagnostics and karyotyping for enhanced detection of chromosomal abnormalities in fetuses. [PDF]

Arch Med Sci
Sun S, Liu C, Lan X, Tang Y.
europepmc   +1 more source

Prenatal Exome Sequencing Analysis in Fetuses With Structural Anomalies: A Multicenter Prospective Cohort Study With Practical Implications

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To evaluate the diagnostic value of prenatal exome sequencing (ES) integrated with copy number variant (CNV) and single nucleotide variant (SNV) analysis (ES‐CNV/SNV) in fetuses with structural anomalies following negative chromosomal microarray analysis (CMA) and karyotyping, and to delineate the practical challenges encountered ...
Yulin Jiang, Haibo Li, Xiangyu Zhu, Liangpu Xu, Ying Chang, Fengqun Dong, Jianping Xiao, Jian Gao, Minyue Dong, Ying Peng, Hua Jin, Ting Wang, Xiaoxiao Xie, Lin Zhang, Hongmei Zhuang, Na Hao, Xiya Zhou, Hongna Wang, Ying You, Kun Ma, Rui Xiao, Qingwei Qi   +21 more
wiley   +1 more source

Differentiating Imaging Characteristics of Congenital Diaphragmatic Hernia and Diaphragmatic Eventration. [PDF]

J Multidiscip Healthc
Ji SH, Zhang H, Li Z, Niu SL, Han MR.
europepmc   +1 more source

Novel LPIN2 mutations in Majeed syndrome induce NF‐κB pathway activation

Rheumatology &Autoimmunity, EarlyView.
This study identifies novel LPIN2 mutations in Majeed syndrome that induce NF‐κB pathway activation, linking defective LPIN2 function to aberrant inflammation in this rare autoinflammatory disorder.
Yibing Han, Renmei Cai, Yuanxuan Ma, Shiguo Liu, Bin Liu   +4 more
wiley   +1 more source

Prenatal ultrasonography and genetic analysis of fetal cleidocranial dysplasia: A case report.

World J Clin Cases
Wang F, Dai PF, Gao WJ.
europepmc   +1 more source

Prenatal suspicion and ultrasound diagnosis of umbilical artery thrombosis: A case report with targeted Doppler evaluation and timely delivery. [PDF]

Medicine (Baltimore)
Li G, Yin X, Guo J, He Y.
europepmc   +1 more source