Results 61 to 70 of about 6,378 (227)

Fetal Brain Abnormalities in Trisomy 21 and Associated Neurodevelopmental Outcome: Key Factors to Identify Differences in Neurodevelopmental Outcome?

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective Trisomy 21 (T21) is associated with various neurological impairments. However, the mechanisms of fetal brain development in T21 and their impact on neurodevelopmental outcomes remain unclear, limiting prenatal counseling. Therefore, this study aims to assess neuropathological changes in fetuses with T21 and the associated ...
Christina Haberl, Pilar Palmrich, Eva Karner, Patric Kienast, Sarah Glatter, Florian Heinzl, Philipp Moser, Daniela Prayer, Gregor Kasprian, Julia Binder   +9 more
wiley   +1 more source

Incidental finding of maternal malignancy in an unusual non‐invasive prenatal test and a review of similar cases

Clinical Case Reports, 2022
We present a clinical case where a complex abnormal non‐invasive prenatal test (NIPT) result in a research project revealed carcinoma of the breast in the pregnant woman.
Maria Hammer Moellgaard, Ida Charlotte Bay Lund, Naja Becher, Anne‐Bine Skytte, Lotte Andreasen, Malgorzata Ilona Srebniak, Ida Vogel   +6 more
doaj   +1 more source

Genetic Investigation in Fetal Growth Restriction: An Integrated Approach for Clinical Practice

Prenatal Diagnosis, EarlyView.
ABSTRACT International guidelines recommend genetic testing when fetal growth restriction (FGR) accompanies structural anomalies, but recommendations for apparently isolated FGR remain variable, particularly regarding gestational age thresholds and the role of exome sequencing (ES). Interpretation is difficult because studies define FGR inconsistently,
Eran Ashwal, David Chitayat
wiley   +1 more source

Influence of Central Sensitisation on Posture, Stability, and Walking Among Individuals with Non-Specific Chronic Low Back Pain

International Journal of Physiotherapy
Background: Non-specific chronic low back pain (NSCLBP) is a prevalent musculoskeletal condition often associated with central sensitisation, which amplifies pain perception and disrupts sensory processing, motor control, and postural regulation.
Manasa Kolekar, Nityal Kumar Alagingi
doaj   +1 more source

Understanding knowledge, perception, and willingness of non-invasive prenatal testing for fetal aneuploidy: a survey among Chinese high-risk pregnant women

Frontiers in Medicine, 2023
ObjectivesNon-invasive prenatal testing (NIPT) is utilized for screening the likelihood of fetal aneuploidy, presenting the benefits of non-invasiveness, high sensitivity, and specificity. Its application in prenatal screening has become ubiquitous.
Yi Zhao, Zhu Xue, Yarui Geng, Jie Zhu, Maidan Hu, Minmin Jiang   +5 more
doaj   +1 more source

The Influence of Parenting Style on Neurocognitive Development of Children With an Extra X or Y Chromosome: A Prospective 1‐Year Follow‐Up Study

Andrology, EarlyView.
ABSTRACT Background As sex chromosome trisomies (SCTs), including 47, XXX, 47, XXY, and 47, XYY, are associated with increased risk for neurodevelopmental challenges, studying SCTs may help in understanding the role of early parental caregiving in shaping neurodevelopmental phenotypes of this genetically at‐risk population.
Sophie van Rijn, Nienke Bouw, Kimberly Kuiper, Evelien Urbanus, Hanna Swaab   +4 more
wiley   +1 more source

Effectiveness of Neurodevelopmental Therapy on Pelvic Alignment, Trunk Control, and Gait Parameters in Chronic Stroke Individuals: A Randomized Controlled Trial

International Journal of Physiotherapy
Background: Stroke is a common neurological disorder that is exclusively due to vascular causes and is characterized by the quick onset of localized disturbance of brain function that results in death and disability.
Jayashree, Rakesh Krishna Kovela
doaj   +1 more source

Prevalence of Spermatozoa in the Ejaculate of Adolescents With Klinefelter Syndrome: Implications for Fertility Counseling

Andrology, EarlyView.
ABSTRACT Background Klinefelter syndrome (KS) is the most common genetic cause of male infertility and is associated with nonobstructive azoospermia. Advances in surgical sperm retrieval techniques have enabled biological fatherhood in a subset of men with KS.
Cecilie N. Larsen, Andrés Felipe Ø. Fritzbøger, Sofia B. Winge, Niels Jørgensen, Anders Juul, Lise Aksglaede   +5 more
wiley   +1 more source

Discordant prenatal and postnatal RhD typing caused by a novel RHD frameshift variant (c.540del; p.Leu181CysfsTer48) in Swedish individuals

Vox Sanguinis, EarlyView.
Abstract Background and Objectives Non‐invasive prenatal testing (NIPT) for fetal RHD genotyping is widely used to guide anti‐D prophylaxis, but discrepancies between predicted fetal RhD status and postnatal serological typing can occur due to variant RHD alleles.
Ahlam Badri, Dan Gratschev, Tove Johansson, Agneta Wikman, Tesfai Emahazion   +4 more
wiley   +1 more source

Coexistence of Suspected Tetralogy of Fallot With Absent Pulmonary Valve and Dextrocardia in Pre‐Gestational Diabetes Mellitus: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Early fetal echocardiography and serial surveillance are crucial in pregnancies complicated by pregestational diabetes. Tetralogy of Fallot with absent pulmonary valve syndrome may cause progressive cardiomegaly, ventricular hypertrophy, hydrops, and fetal demise.
Alireza Golbabaei, Vida Kahani, Marzieh Mousivand   +2 more
wiley   +1 more source