Results 21 to 30 of about 5,099,040 (214)

The role and tasks of the midwife in the care of a patient during pregnancy complicated by intrauterine growth retardation

Medycyna Ogólna i Nauki o Zdrowiu, 2020
Introduction Intrauterine growth retardation (IUGR) is a result of mutual influence and interaction of etiological factors. Pathological foetal development dynamic, mismatched with gestational age, is a direct threat to the viability of pregnancy and is ...
Małgorzata Stefaniak, Ewa Anna Dmoch-Gajzlerska   +1 more
doaj   +1 more source

Fetal renal hyperechogenicity in intrauterine growth retardation : importance and outcome. [PDF]

, 2001
peer reviewedThe object of the study was to investigate the outcome in growth-retarded newborns who were diagnosed with fetal renal hyperechogenicity without anatomical abnormality during any stage of pregnancy.
Foidart, Jean-Michel, Suranyi, A., Retz, C., Schaaps, Jean-Pierre, Rigo, Jacques   +4 more
core   +1 more source

Chromosomal aberrations as etiological factors of intrauterine growth retardation [PDF]

Vojnosanitetski Pregled, 2008
Background/Aim. Intrauterine growth retardation (IUGR) is a pathological condition of pregnancy characterised by birth weight below the 10th centile. A number of fetal, placental and maternal causes can lead to IUGR; although, in most cases no specific ...
Petrović Bojana, Ljubić Aleksandar, Nikolić Ljubinka   +2 more
doaj   +1 more source

Congenital Cytomegalovirus in Algiers, Algeria, a Descriptive Case Series Study

Journal of Medical Microbiology and Infectious Diseases, 2022
Cytomegalovirus (CMV) is an endemic ubiquitous herpes virus transmitted through saliva, urine, genital secretions, mononuclear blood cells, and transplanted tissue.
Samira AGGOUNE1*
doaj   +1 more source

Forest diagram of the relationship between intrauterine growth retardation and the incidence of MBDP.

, 2022
Forest diagram of the relationship between intrauterine growth retardation and the incidence of MBDP.
Changjun Ren (10885182), Jinfeng Meng (3499739), Shangbin Li (10885176), Ling Hao (193154), Jie Wang (16762), Baochang Chen (12867492), Jingfei Sun (12867495), Qian Zhao (217607), Weichen Yan (10885179), Jiayu Huang (3408389)   +9 more
core   +1 more source

Epigenetic changes predisposing to type 2 diabetes in intrauterine growth retardation.

Frontiers in Endocrinology, 2010
Epidemiologic studies have demonstrated an association between intrauterine growth retardation and a greater risk of chronic disease, including coronary heart disease, hypertension, stroke, and type 2 diabetes in adulthood.
Alice eLiguori, Antonella ePuglianiello, Daniela eGermani, Annalisa eDeodati, Emanuela ePeschiaroli, Stefano eCianfarani   +5 more
doaj   +1 more source

Serum lipids in newborns with intrauterine growth retardation

, 2000
Background: The X syndrome, related to coronary disease in adults, could be possibly programmed priory to delivery, in children with intrauterine growth retardation.
Casanueva E,Víctor, Pérez V,Ruth, Venegas B,Héctor, Cid S,Luis, Molina S,Marta, Dios T,Gabriela, Reyes R,Marina, Ferrada N,María Cristina   +7 more
core   +1 more source

An Injectable, Self‐Expanding Hemostatic Foam for Field‐Compatible Postpartum Hemorrhage Management

Advanced Science, EarlyView.
Postpartum hemorrhage is the leading cause of maternal death worldwide, yet many treatments are hard to use outside well‐equipped hospitals. This work introduces an easy‐to‐use device that rapidly delivers a degradable foam into the uterus. The foam stops bleeding through pressure and clotting support, offering a practical option for low‐resource ...
Charlotte Meyer, Noël Strasser, Ilakkiya Ravindrarajah, Elsa Wrenger, Kristian Ivkovic, Jan Ševčík, Sima Šarčević, Lenka Červenková, Jáchym Rosendorf, Václav Liška, Alexandre H. Anthis, Thomas Rduch, Inge K. Herrmann   +12 more
wiley   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source

Intrauterine growth retardation and fetal cardiac function

, 2000
Intrauterine growth retardation is a pathology which is found in 3–10% of all pregnancies and it is associated with around 20–25% of all fetal intrauterine deaths and with long-term neurologic sequelae.
Verzuri, M. S., Bocchi, C., Severi, Filiberto Maria, D'Antona, Donato, Severi, F. M., Arduini, D., G. RIZZO, Rizzo, G., Bocchi, Caterina, Verzuri, M.S., D'Antona, D., D. ARDUINI, Rizzo, Giuseppe, Arduini, Domenico, F. M. SEVERI, C. BOCCHI, M. S. VERZURI   +16 more
core   +1 more source