Tag: #CongenitalAnomalies
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Genetic Studies in Assisted Reproduction Unveiling the Risk of Congenital Anomalies
Introduction The journey to parenthood through assisted reproductive technologies (ART) has transformed the lives of countless couples worldwide. However, concerns about the potential risk of congenital anomalies among children conceived through in vitro fertilization (IVF) continue to spark important scientific discussions. A recent observational study conducted by researchers from the National and Kapodistrian University of…
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Unveiling Patterns in Fetal Malformations Insights from a Multi Center Observational Study
Introduction Understanding congenital anomalies is vital to shaping maternal-fetal healthcare. A recent multi centric study conducted at Beni Suef University Hospital sheds light on the prevalence and types of fetal malformations observed among over 20,000 pregnant women.Visit https://www.obstetricgynecoljournal.com for more groundbreaking research in the field of obstetrics and gynecology. Main Findings and Key Highlights Public…
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A Fatal Diagnosis in the Womb Understanding Meckel Gruber Syndrome and Its Devastating Implications
Introduction Among the rare congenital anomalies that challenge prenatal medicine, Meckel Gruber Syndrome (MGS) stands out as one of the most lethal. Characterized by severe malformations in the brain, kidneys, and limbs, MGS presents heartbreaking decisions for expecting parents. A recent case report published in Clinical Journal of Obstetrics and Gynecology adds valuable insight to…
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Understanding Persistent Oropharyngeal Membrane in Calves: A Rare Developmental Anomaly
Introduction Persistent oropharyngeal membrane is a rare congenital anomaly affecting the oral and pharyngeal regions in animals, including calves. A recent case study published in Archives of Case Reports examines a calf diagnosed with this condition, providing crucial insights into its clinical, histopathological, and surgical evaluations. Visit https://www.hspioa.org/ for more groundbreaking research in this field.…
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A Rare Case Congenital Megalourethra in Prune Belly Syndrome
Introduction Prune Belly Syndrome (PBS) is a rare congenital disorder affecting approximately 1 in 40,000 male births. It is characterized by a triad of symptoms: abdominal muscle deficiency, undescended testicles, and urinary tract abnormalities. In this case study, we explore an unusual presentation of PBS associated with congenital megalourethra. For more groundbreaking research in this…
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