Results 1 to 10 of about 796 (160)
Evaluation of the Results of Cordocentesis
Taiwanese Journal of Obstetrics and Gynecology, 2007 Objective: To evaluate the results of cordocentesis carried out in our clinic at Meram Medicine Faculty of Selcuk University in Konya, Turkey. Materials and Methods: Cytogenetic results and complication data were obtained by cordocentesis from 250 ...
Kazim Gezginç, Osman Balcı
exaly +6 more sources
Prevention is Better than Cure! Can We prevent Primary Immune Deficiency Diseases? [PDF]
Pediatric Infectious Disease, 2023 Severe immune deficiencies are often fatal in young childhood unless recognized and treated with a hematopoietic stem cell transplant (HSCT) timely. The majority of the immune deficiencies are monogenic diseases and may affect multiple children in the ...
Prerna Jhawar, Neha Singh, Sagar Bhattad
doaj +1 more source
Clinical and Experimental Obstetrics & Gynecology, 2023 Background: To evaluate the safety profiles and role of antepartum transabdominal amnioinfusion (TA) in detecting fetal anomalies in pregnant women with oligohydramnios during the second trimester.
Wei Gu +5 more
doaj +1 more source
Prenatal Diagnosis for Primary Immunodeficiency Disorders—An Overview of the Indian Scenario
Frontiers in Immunology, 2020 Prenatal Diagnosis (PND) forms an important part of primary preventive management for families having a child affected with primary immunodeficiency.
Reetika Malik Yadav +33 more
doaj +1 more source
Rh disease: intrauterine intravascular fetal blood transfusion by cordocentesis
The Turkish Journal of Pediatrics, 1999 A total of 49 cordocenteses, including 40 intrauterine intravascular fetal blood tranasfusions, were performed in 30 pregnancies complicated by red cell isoimmunization.
Lütfü Önderoğlu, Cem Öncüloğlu
doaj +1 more source
Managing Severe Foetal Anaemia Due to Rh Alloimmunisation: A Report of Two Cases of Successful Intrauterine Blood Transfusion [PDF]
Journal of Clinical and Diagnostic ResearchIntrauterine Transfusion (IUT) remains a critical intervention in managing severe foetal anaemia, particularly due to Red Blood Cell (RBC) alloimmunisation.
B Megala +4 more
doaj +1 more source
Molecular Cytogenetics, 2020 Background Cordocentesis in our practice is most commonly indicated for rapid karyotyping in the second or third trimester and is regarded as the gold standard for foetal chromosomal aberration diagnosis in pregnancies at high risk for chromosomal ...
Yanmei Sun +6 more
doaj +1 more source
Relevance of Invasive Testing in Era of Non-Invasive Testing for Prenatal Chromosomal Abnormalities
Gynecology Obstetrics & Reproductive Medicine, 2022 Prenatal screening for chromosomal abnormalities has two components i.e. prenatal screening (maternal serum screening and cell-free fetal DNA screening) and prenatal diagnosis (chorionic villus sampling, amniocentesis, and cordocentesis).
Abhijeet Kumar +2 more
doaj +1 more source
Prenatal Diagnosis of Mosaic Tetrasomy 18p in a Case without Sonographic Abnormalities [PDF]
International Journal of Molecular and Cellular Medicine, 2017 Small supernumerary marker chromosomes (sSMC) are still a major problem in clinical cytogenetics as they cannot be identified or characterized unambiguously by conventional cytogenetics alone.
Javad Karimzad Hagh +8 more
doaj
Non-Invasive Screening Test Paradox in a Case Born with Mixed Gonadal Dysgenesis (45,X/46,Xy)
Balkan Journal of Medical Genetics, 2023 Noninvasive prenatal testing (NIPT) is commonly used to screen for fetal trisomy 13, 18, and 21 and often for sex chromosomal aneuploidies (SCAs). Although the testing is also used for sex chromosomal aneuploidies, it is not as efficient as it is for ...
Cobanogullari H., Akcan N., Ergoren M.C.
doaj +1 more source