Results 91 to 100 of about 12,929 (176)

The Role of Continuous Glucose Monitoring in Managing Hyperglycaemia First Detected in Pregnancy: A Narrative Review

Diabetes, Obesity and Metabolism, Volume 28, Issue 9, Page 7719-7736, September 2026.
ABSTRACT Hyperglycaemia first diagnosed in pregnancy (HIP) is the most common medical condition affecting pregnancy, affecting up to 40% of pregnancies in some countries. The global incidence of HIP is increasing owing to rising rates of overweight and obesity, advanced maternal age, and early screening for HIP.
Emmanuel Cosson, Laura Chabrol Haas, Fleur Levrat‐Guillen   +2 more
wiley   +1 more source

Macrosomía fetal y su impacto en la salud pública

Revista Internacional de Salud Materno Fetal, 2016
Este artículo va especialmente dedicado a ustedes, nuestros lectores, que nos han acompañado en una edición más de nuestra revista Yo Obstetra y que juntos hemos crecido en conocimientos y aprendido nuevas cosas.
Bruma Esmeralda Vega Amador
doaj  

Determinants of macrosomia among newborns delivered in Jigjiga City, Eastern Ethiopia: a case-control study

Maternal Health, Neonatology and Perinatology
Background Macrosomia is a forgotten health problem that directly or indirectly affects maternal and neonatal health outcomes. There is a lack of evidence on the factors that affect macrosomia in eastern Ethiopia.
Abdisalan Elmi Farah, Dureti Abdurahman, Kassiye Shiferaw, Ahmedin Aliyi Usso, Mohammed Abdurke Kure, Beker Feto, Hassen Abdi Adem, Saba Hailu   +7 more
doaj   +1 more source

Malectin Alleviates Endoplasmic Reticulum Stress in Gestational Diabetes Mellitus via Glycoprotein Quality Control Mechanisms

Advanced Science, Volume 13, Issue 46, 17 August 2026.
Malectin alleviates high glucose‐induced ER stress and damage in placental trophoblasts, a function dependent on its six critical carbohydrate‐binding residues. In a GDM mouse model, administration of TAT‐Malectin ameliorated hyperglycemia and placental ER stress and prevented fetal macrosomia.
Jiahui Zhu, Yumeng Zhang, Ye Wang, Xiaoyu Zhu, Ailin Yuan, Weijing Yin, Huangmin Yu, Xuemin Pang, Yufeng He, Yuchen Wang, Tong Wang, Yong Li, Yunlong Si   +12 more
wiley   +1 more source

Macrosomía fetal en madres no diabéticas. Caracterización mínima

Medisan, 2013
Por macrosomía se entiende el desarrollo del cuerpo a tamaño exagerado, debido a diversas causas. Respecto a la madre y a su hijo también son diferentes los factores de riesgo que les afectan; por ello se efectuó un estudio retrospectivo y transversal ...
Abelardo Salvador Toirac Lamarque, Viviana Pascual López, Asdrúbal Martínez Jiménez, Rosa Isabel Area Suárez   +3 more
doaj  

The 9th International RASopathies Symposium

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1934-1941, August 2026.
ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel, Lisa Schoyer, Beth Stronach, Raya Bogdanova, Anton M. Bennett, Jaishri Blakeley, Miriam Bornhorst, Tammy Bowers, Saskia M. Brachmann, Emma Burkitt‐Wright, Kathryn Chatfield, Alessandro De Luca, Khalil El‐Chammas, Abdul Elkadri, John E. Fortunato, Bruce D. Gelb, Anne Goriely, Karen Gripp, Kassidy Grover, Lindsay Homan, Kenneth A. Kern, Maija Kiuru, Charles (Chuck) Lawson, Yong‐Seok Lee, Frank McCormick, Gina Ney, Cristina Nuevo‐Tapioles, Sara Pardej, Elizabeth I. Pierpont, Julia Plank, Nancy Ratner, Katherine A. Rauen, J. Elliott Robinson, Les Rogers, Sarah E. Sheppard, Keir Shiels, David Stevenson, Dagmar Tiemens, Matthew Traylor, K. Nicole Weaver, Marielle Yohe, Tamar Green   +41 more
wiley   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1783-1798, August 2026.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet, Sylvie A. Adams, Zoe S. Katz, Christal G. Delagrammatikas, Kosuke Izumi, Winifred Sigal, Kim Ventarola, Elaine H. Zackai, Julia E. Reid, Grant T. Liu, Jennifer M. Kalish   +10 more
wiley   +1 more source

Pre‐Eclampsia and Its Associated Factors Among Pregnant Women in Ghana: A Retrospective Study

Health Science Reports, Volume 9, Issue 8, August 2026.
ABSTRACT Background and Aims Pre‐eclampsia remains a major cause of feto‐maternal death in Ghana, with a rising incidence linked to multiple factors that hinder prevention. Despite it's impact, few studies have explored associated risks. This study assessed the prevalence, risk factors, and maternal–neonatal outcomes associated with pre‐eclampsia among
Sabastian Adjei, Wilfred Sam‐Awortwi Jnr, Richmond Adu Boahen Boamah, Edward Osei Gyimah, William Kweku Payne, Harriet Yeboaa Diawuo, Samuel Kwame Sopuruchi Agomuo, Oscar Simon Olympio Mensah, Alfred Effah, Christian Obirikorang   +9 more
wiley   +1 more source

The FemTech revolution: Unlocking the potential of new technology for optimizing pregnancy outcomes in low‐ and middle‐income countries and remote areas

International Journal of Gynecology &Obstetrics, Volume 174, Issue 2, Page 530-553, August 2026.
Abstract Maternal and neonatal mortality and morbidity rates uncover major global health disparities. Despite ongoing efforts, the rates of maternal and neonatal complications remain substantially higher in low‐ and middle‐income countries (LMICs) compared to high‐income countries (HICs). These high rates are the result of several unmet needs in LMICs,
Nir Melamed, Hema Divakar, Mahesh Choolani, Fionnuala M. McAuliffe, Lin Foo, Hassan Shehata, Gabriel Jones, Vyta Senikas, Eline M. Van der Beek, Nandita Palshetkar, Gabriele Saccone, Vincenzo Berghella, Mauricio A. Cuello, Justin Konje, Bhaskar Bhatt, Augusto Cam, Moses Obimbo, Aris Papageorghiou, Moshe Hod, on behalf of the FIGO Committee on Women's Health and Technology   +19 more
wiley   +1 more source

Prenatal Genetic Testing for Beckwith‐Wiedemann Syndrome: Considerations, Challenges and Observations (A Real‐World Study)

Prenatal Diagnosis, Volume 46, Issue 9, Page 1486-1493, August 2026.
ABSTRACT Objective Prenatal genetic testing for imprinting disorders is rarely requested with the exception of Beckwith‐Wiedemann syndrome (BWS) which is associated with specific ultrasound findings (e.g., placental mesenchymal dysplasia, omphalocele). However, genetic testing for BWS is challenging as aberrant DNA methylation has to be addressed which
Melissa Connolly, Louise McClelland, Pierpaola Tannorella, Tanja Richter, Ester Mainini, Andreas Dufke, Annette Lischka, Matthias Begemann, Katja Eggermann, Thomas Eggermann, Silvia Russo   +10 more
wiley   +1 more source