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Indications of Amniocentesis and its Early and Late Complications.
Adv Biomed Res
October 2024
Department of Obstetrics and Gynecology, Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Background: Currently, it is recommended to arrange screening for all women who are referred for prenatal care before the 20 week of gestation. Congenital and genetic diseases lead to disability and death in 3% of babies. Prenatal diagnosis is the only way to prevent the birth of babies with genetic disorders.
View Article and Find Full Text PDFFetal Alcohol Spectrum Disorder and Pediatric Neurology: Are We Missing the Connection? A Scoping Review.
J Child Neurol
December 2024
Harley French Medical Library, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND, USA.
Introduction: Pediatric neurology provides care for children with complex developmental disorders with environmental, genetic, metabolic, and teratogenic etiologies. Common neurodevelopmental conditions include attention-deficit hyperactivity disorder (ADHD), and autism spectrum disorder. However, only minimal attention from pediatric neurology journals has been devoted to fetal alcohol spectrum disorder.
View Article and Find Full Text PDFFeasibility Versus Success: Bridging the Evidence Gap in Endoscopic Third Ventriculostomy for Fetal Interventions.
Prenat Diagn
December 2024
Division of Maternal-Fetal Medicine and Surgery, Fetal Care and Surgery Center, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
In Response to the Letter by Dr. Shamshirsaz and Colleagues: "Feasibility Versus Success: Bridging the Evidence Gap in Endoscopic Third Ventriculostomy for Fetal Interventions.".
Prenat Diagn
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HCor, Hospital do Coração de Sao Paulo, Sao Paulo, Brazil.
Genetic analysis of partial duplication of the long arm of chromosome 16.
BMC Med Genomics
December 2024
Department of Pediatrics, Sichuan Provincial Woman's and Children's Hospital, The Affiliated Women's and Children's Hospital of Chengdu Medical College, Chengdu, China.
Background: Pure partial trisomy 16q12.1q22.1 is a rare chromosome copy number variant (CNV).
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