Results 161 to 170 of about 725,003 (400)

Hysterotomy for Retained Placenta in a Septate Uterus: A Case Report

Case Reports in Obstetrics and Gynecology, 2012
Retained placenta is a common complication of the third stage of labor. Most literature has focused on management of a trapped placenta or placenta accreta.
Daniel Lee, Joseph Johnson
doaj   +1 more source

Clinically Irrelevant Terminal 16q21 Deletion Detected by NIPT Is Attributable to Inherited Fragility at FRA16B

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genome‐wide non‐invasive prenatal testing (NIPT) is a powerful tool for prenatal detection of the common aneuploidies causing Down‐, Edwards‐, and Patau syndrome. Its genome‐wide reach also enables the detection of unbalanced structural chromosomal abnormalities.
Servi J. C. Stevens, Wanwisa van Dijk, Nicole Y. Souren, Merryn V. E. Macville, Guillaume van de Zande, Brigitte H. W. Faas, Bart de Koning, Arthur van den Wijngaard, Sonja de Munnik, Masoud Zamani Esteki   +9 more
wiley   +1 more source

PLACENTA ACCRETA – RISK FACTORS, SURGICAL AND CLINICAL OUTCOME [PDF]

Journal of IMAB
Placenta accreta is a spectrum of antenatal diagnostic markers, surgical complications and life-threatening diagnoses. Objective: To evaluate the risk factors, the surgical complications and the clinical peripartal outcomes in the placenta accreta ...
Mariana Tsankova, Sergei Slavov, Ivan Kostov   +2 more
doaj   +1 more source

Defense and infection of the human placenta

Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS), 2018
The placenta functions as a shield against infection of the fetus. The innate and adaptive immune defenses of the developing fetus are poorly equipped to fight infections.
Amy E Heerema-McKenney
semanticscholar   +1 more source

New Insights Into Changes in the DNA Methylation Pattern of the SHOX Gene in Patients With Léri‐Weill Dyschondrosteosis

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT SHOX gene haploinsufficiency is associated with Léri‐Weill dyschondrosteosis (LWD) or idiopathic short stature (ISS) and could be caused by the structural and point mutations in the coding region and by the deletions in SHOX gene regulatory sequences. The role of the duplications in regulatory sequences is ambivalent.
Valeriia Kopytko, Katerina Hirschfeldova, Pavlina Capkova, Roman Solc   +3 more
wiley   +1 more source

Editorial: Immunological challenges around pregnancy complications associated with failures of maternal tolerance to the fetus

Frontiers in Immunology, 2022
Michael Eikmans, Diana M. Morales-Prieto, Marie-Louise van der Hoorn, Udo R. Markert   +3 more
doaj   +1 more source

Non‐Invasive Prenatal Testing by Cell‐Free DNA (cfNIPT) for Detecting Turner Syndrome With Mosaicism and Structural Variants—Prenatal Findings and Postnatal Outcomes

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Turner Syndrome (TS) is a sex chromosomal disorder associated with karyotype heterogeneity. Although TS can be associated with severe prenatal findings, most often linked to the 45, X karyotype, the majority of TS fetuses have no overt phenotype, resulting in delayed diagnosis and management.
Ivonne Bedei, Johanna Bruder, Ida C. B. Lund, Simon H. Thomsen, Ida Vogel, Andrea T. Maciel‐Guerra, Francisco Alvarez‐Nava, Melissa L. Crenshaw, Roland Axt‐Fliedner, Claus H. Gravholt, Anne Skakkebæk   +10 more
wiley   +1 more source

Management of Cardiovascular Health Issues in Turner Syndrome: Expert Insights and Expanded Recommendations From the 2024 Guideline Development Team

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Turner syndrome (TS) is frequently complicated by congenital heart disease (CHD). While left‐sided lesions such as bicuspid aortic valve (BAV) and coarctation of the aorta are the most common structural heart lesions in TS, other anomalies, such as aortic arch malformations, hypoplastic left heart syndrome (HLHS), persistent left superior vena
Katya de Groote, Sheetal R. Patel, Kristian Havmand Mortensen, Isabel Witvrouwen, Anthonie Duijnhouwer, Nicole M. Brown, Jasmine Grewal, Kathryn C. Chatfield, Aaron T. Dorfman, Siddharth K. Prakash   +9 more
wiley   +1 more source

Efecto sobre la función trofoblástica in vitro, de los anticuerpos antifosfolípidos de pacientes con diferentes manifestaciones clínicas del síndrome antifosfolípido

Iatreia, 2013
INTRODUCCIÓN: el síndrome antifosfolípido (SAF) se define como episodios trombóticos y/o morbilidad gestacional asociados a la presencia de anticuerpos antifosfolípidos (aAFL).
Yonhatan Ramírez Castillo, Ángela Álvarez, Norman Bálcazar, Manuela Velásquez, Beatriz Peña, Udo Markert, Angela Cadavid   +6 more
doaj  

Uterine Mole Showing Low Implantation of the Ovum (Placenta Prævia) [PDF]

, 1913
Thomas Watts Eden
openalex   +1 more source