Littérature scientifique sur le sujet « Hydropsy fetalis »

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Articles de revues sur le sujet "Hydropsy fetalis"

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Pejic, Katarina, Borisav Jankovic, Zeljko Mikovic, Zorica Rakonjac, Jelena Martic, and Natasa Stajic. "Non-immune hydrops fetalis: Clinical experience in newborn infants." Medical review 64, no. 9-10 (2011): 507–10. http://dx.doi.org/10.2298/mpns1110507p.

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Introduction. Non-immune hydrops fetalis is a condition of excessive accumulation of extravascular fluid without identifiable circulating antibody to erythrocytes membrane antigens. In newborn infants it is characterized by skin oedema and pleural, pericardial or peritoneal effusion. In the era of routine Rh immunization for the prevention of foetal erythroblastosis, non-immune pathophysiologic mechanisms are presented in 76-87% of all hydropic newborns. Non-immune hydrops fetalis can be associated with numerous and various disorders. The mortality rate may exceed 50%. This study was aimed at
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Srinivas, G., D.V. Ramanjaneyulu, E. Muralinath, et al. "An Essential Parameters of Parvo Virus Include Patho Physiology, Histo Pathology, Diagnosis, Differential Diagnosis, Treatment and Prognosis." Journal of Research and Reviews in Nursing Science and Education 2, no. 2 (2025): 11–17. https://doi.org/10.5281/zenodo.15541791.

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<em>One virus that only affects people is parvovirus B19. The fifth illness, also known as erythema infectious or slapped cheek syndrome, is known to be caused by it. It primarily affects young children, though it can sometimes affect adults. In addition, it may result in Poly arthropathy, popular-purpuric gloves and socks syndrome (PPGSS) in young people, certain anemias, hydrops fetalis, particularly in pregnant women, and an aplastic crisis. Viral transmission occurs through both respiratory secretions and blood products. The virus can infect a pregnant woman and then infect her unborn chil
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Das, Niladri, Sushma Malik, Prachi Gandhi, Vinaya A. Singh, and Poonam Wade. "Non-immune hydrops fetalis: a case series." International Journal of Contemporary Pediatrics 7, no. 5 (2020): 1195. http://dx.doi.org/10.18203/2349-3291.ijcp20201661.

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Hydrops fetalis is a clinical condition characterized by pathological fluid accumulation in soft tissues and serous cavities of the fetus like peritoneal cavity, pleural cavity, pericardial space, and body wall edema. Hydrops fetalis is broadly classified into Immune Hydrops Fetalis (IHF) and Non-Immune Hydrops Fetalis (NIHF). Incidence of immune hydrops fetalis due to Erythroblastosis fetalis secondary to Rh Iso-immunisation has drastically reduced due to widespread use of anti-D immunoglobulin. In the last few decades, the majority of cases are identified as non-immune hydrops. It is importa
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Krasniqi, Faton, Edmond Pistulli, Astrit M. Gashi, and Isabere Krasniqi. "Non-immunologic hydrops fetalis and coronavirus disease (COVID-19) – A case report." Romanian Journal of Pediatrics 70, no. 1 (2021): 75–79. http://dx.doi.org/10.37897/rjp.2021.1.14.

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Non-immune hydrops fetalis is a severe fetal condition defined as the excessive accumulation of fetal fluid within the fetal extravascular compartments and body cavities. The prevalence of non-immune hydrops fetalis is unknown. Currently, about 90% of cases of hydrops fetalis are non-immune hydrops fetalis. Non-immune hydrops fetalis causes are multi-factorial. The pathophysiological mechanism of non-immunologic hydrops fetalis is related to abnormal fluid transportation between plasma and tissues. This is due to the increase in hydrostatic capillary pressure and capillary permeability and a r
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Yuan, Shi-Min. "Cardiac Etiologies of Hydrops Fetalis." Zeitschrift für Geburtshilfe und Neonatologie 221, no. 02 (2017): 67–72. http://dx.doi.org/10.1055/s-0042-123825.

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AbstractCardiac etiologies of hydrops fetalis have been a topic of concern due to challenging perinatal management. The common cardiac etiologies leading to hydrops fetalis include structural cardiac anomalies, cardiac dysrhythmias, cardiac tumors, cardiomyopathy and myocarditis. The mechanisms of cardiogenic hydrops fetalis may be: 1) elevation of atrial pressure and volume overload, 2) decrease of cardiac output, and 3) development of congestive heart failure. The diagnosis of hydrops fetalis was usually made at 19–36 gestational weeks, when ultrasound is a highly effective diagnostic method
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Lonsdale, Angela. "Hydrops Fetalis." Canadian Journal of Medical Sonography 1, no. 2 (2010): 9–12. http://dx.doi.org/10.3138/cjms.v1i2.9.

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Hydrops fetalis is a complex and fascinating disorder. This article explains the characteristics of each type of hydrops fetalis, immune and non-immune. The etiology and the associated underlying conditions leading to the development of these disorders are also discussed. The ultrasonographic appearance of a classic case of hydrops fetalis is described including variations in its appearance and its numerous differential diagnoses. Several causes of non-immune hydrops fetalis are outlined and briefly discussed. The article concludes with delivery recommendations and discusses a future plan of a
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Oliver, Kate E., Kimberly W. Hickey, and Scott M. Petersen. "Spontaneous Resolution of Mirror Syndrome following Demise of Hydropic Twin." Case Reports in Obstetrics and Gynecology 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/783408.

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Maternal mirror syndrome is a rare consequence of fetal hydrops. By convention, delivery is recommended in pregnancies complicated by mirror syndrome due to grave fetal prognosis. We describe a case of a dichorionic, diamniotic twin gestation complicated by hydrops fetalis of twin B. The patient declined selective feticide. Two weeks later, intrauterine fetal demise of fetus B was diagnosed and complete resolution of mirror syndrome followed. Unaddressed, mirror syndrome can lead to significant maternal and fetal complications. This case illustrates resolution of mirror syndrome following spon
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González González, Luis Alberto, Zaida Selene Zamora Chávez, Katya Miroslava Mora Rivera, Maria Elizabeth Jimenez Ahumada, and Maria Tsuyuko Shiguematsu. "Caso Clínico: Hydrops Fetal No Inmune." Estudios y Perspectivas Revista Científica y Académica 4, no. 2 (2024): 155–67. http://dx.doi.org/10.61384/r.c.a..v4i2.205.

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Introducción: Se define hydrops fetalis como la presencia de 2 o más colecciones anormales de líquido en el feto, con evidencia mediante ecografía, 9, 11. Estas colecciones de líquido se presentan como ascitis, derrame pleural, derrame pericárdico y edema cutáneo generalizado (con espesor de piel &gt;5 mm), 10, 12. Hay dos categorías de hydrops fetalis: inmune y no inmune. El hydrops fetalis no inmune es específicamente de casos sin aloinmunización con glóbulos rojos, 9. Actualmente se ha repostado que la incidencia de hydrops fetalis inmune a disminuido en los últimos años de manera significa
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Agarwal, Arjit, Shubhra Agarwal, Astha Lalwani, Rehana Najam, and Ashutosh Kumar. "Fetal bradyarrhythmia causing hydrops fetalis: A journey from fetal echo to autopsy." Ultrasound 28, no. 4 (2020): 266–70. http://dx.doi.org/10.1177/1742271x20933996.

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Introduction Non-immune hydrops fetalis is a condition with poor fetal prognosis. The incidence of this clinical condition is increasing as compared to its iso-immune variant. The diagnosis of hydrops fetalis is straightforward; however, delineating the primary cause of non-immune hydrops fetalis requires a holistic approach and background knowledge of the entity. Case report We present a case of non-immune hydrops fetalis due to a rare functional cardiac disorder demonstrated by features of cardiac failure in the form of clinically significant tricuspid regurgitation detected on echocardiogra
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Randenberg, Andrea. "Nonimmune Hydrops Fetalis Part II: Does Etiology Influence Mortality?" Neonatal Network 29, no. 6 (2010): 367–80. http://dx.doi.org/10.1891/0730-0832.29.6.367.

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HYDROPS FETALIS IS A CONDITION in which there is an excess of total body fluid, primarily within the fetal interstitial spaces.1,2 Etymologically, hydrops fetalis is a Latin term meaning “edema of the fetus.”2,3 In addition to generalized edema, the fetus has at least one of the following: ascites, pericardial effusion, pleural effusion(s), and an abnormally thick (&gt;6 cm) placenta.4–6 Hydrops is classified as nonimmune hydrops fetalis (NIHF) when it occurs without evidence of isoimmunization.7,8
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Thèses sur le sujet "Hydropsy fetalis"

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Tolfvenstam, Thomas. "Human parvovirus B19 : studies on the pathogenesis of infection /." Stockholm, 2001. http://diss.kib.ki.se/2001/91-628-4710-4/.

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Moreno, Carolina Araujo 1981. "Estudo da etiopatogenia da hidropisia fetal não-imune a partir de uma série de casos utilizando um protocolo de investigação ampliado." [s.n.], 2013. http://repositorio.unicamp.br/jspui/handle/REPOSIP/308790.

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Orientador: Denise Pontes Cavalcanti<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas<br>Made available in DSpace on 2018-08-22T09:53:23Z (GMT). No. of bitstreams: 1 Moreno_CarolinaAraujo_M.pdf: 4072523 bytes, checksum: 09921eee06d7c1098048c98a3f891b33 (MD5) Previous issue date: 2013<br>Resumo: A hidropisia fetal não-imune (HFNI) é causada por um grupo heterogêneo de condições e atualmente corresponde à maior parte dos casos de hidropisia fetal. Em função da ampla diversidade etiopatogênica, a investigação dos casos de HFNI constitui um desafio dia
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Rudzki, Karin. "Hydrops fetalis zur Pathologie einer speziellen Form der Wassersucht unter besonderer Berücksichtigung von Fallstudien und klinischen Befunden /." [S.l.] : [s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=967527317.

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Weiffenbach, Johannes [Verfasser], and Barbara [Akademischer Betreuer] Gärtner. "Nachweis Parvovirus B19-spezifischer Immunglobulin G und Immunglobulin M Antikörper im Fetalblut in Gegenwart einer Parvovirus B19-induzierten fetalen Anämie oder eines Parvovirus B19-bedingten Hydrops fetalis / Johannes Weiffenbach. Betreuer: Barbara Gärtner." Saarbrücken : Saarländische Universitäts- und Landesbibliothek, 2013. http://d-nb.info/1052955142/34.

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Hendy, K. M. "The effects of gestational age and placental restriction on the expression of 11[Beta] - hydroxy-steroid dehydrogenase in fetal sheep liver and kidney /." Title page and abstract only, 1997. http://web4.library.adelaide.edu.au/theses/09MSB/09msbh498.pdf.

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Haave, Neil Christian. "Sensitivity of hepatic 3-hydroxy-3-methylglutaryl coenzyme A reductase to external stimuli and its relationship to in vivo rates of cholesterol synthesis in the fetal rat." Thesis, University of British Columbia, 1991. http://hdl.handle.net/2429/31011.

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During gestation the fetus requires cholesterol for membrane accretion, steroidogenesis and lipoprotein synthesis. Very little is known, however, about the mechanisms which regulate cholesterol synthesis in the fetus. When the bile-acid binding resin cholestyramine (CY) is fed to rats throughout gestation the activity of fetal hepatic 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase (EC 1.1.1.34, rate-limiting enzyme of cholesterol synthesis in adult rats) increases. CY is not absorbed from the gut into the circulation and therefore cannot cross the placenta. Hence, maternal CY feedi
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Dubbermann, Claudia [Verfasser]. "Fetale Prognose und maternale Risiken bei Hydrops fetalis / vorgelegt von Dubbermann, Claudia." 2004. http://d-nb.info/975008463/34.

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Barros, Filipa Batschelet. "Non-immune Hydrops Fetalis - Experience of a level III Neonatal Intensive Care Unit." Master's thesis, 2017. https://hdl.handle.net/10216/104075.

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Barros, Filipa Batschelet. "Non-immune Hydrops Fetalis - Experience of a level III Neonatal Intensive Care Unit." Dissertação, 2017. https://hdl.handle.net/10216/104075.

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Rudzki, Karin [Verfasser]. "Hydrops fetalis : zur Pathologie einer speziellen Form der Wassersucht unter besonderer Berücksichtigung von Fallstudien und klinischen Befunden / vorgelegt von Karin Rudzki." 2001. http://d-nb.info/967527317/34.

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Livres sur le sujet "Hydropsy fetalis"

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Johannesen, Jennifer. No ordinary boy: The life and death of Owen Turney. Low to the Ground Pub., 2011.

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Breisgau, Universität Freiburg im, ed. Nichtimmunologischer Hydrops fetalis: Prä- und postpartale Befunde. 1991.

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Archer, Nick, and Nicky Manning. Fetal hydrops and the heart. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199230709.003.0020.

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Introduction 270Pathophysiology 275Aetiology 276Assessment and monitoring 278Management 279Hydrops fetalis refers to the pathological condition where fluid collects in 2 or more body cavities; it represents excessive accumulation of interstitial fluid, initially in the serous spaces (pericardial, pleural, and peritoneal cavities—...
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Breisgau, Universität Freiburg im, ed. Der nichtimmunologische Hydrops fetalis (NIHF): Pathophysiologische Überlegungen und 59 Falldarstellungen. 1992.

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Richard, Ina Karin. Vergleichende Untersuchung zu Ätiopathogenese und Letalität des nicht-immunologischen Hydrops fetalis (NIHF). 1993.

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Fox, Grenville, Nicholas Hoque, and Timothy Watts. Fluids and electrolytes. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198703952.003.0005.

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This chapter provides an overview of the background of fluid balance in the neonate, including the need to compensate for fluid loss (output), and the requirement to provide energy and nutrition. It also covers the management of common issues in fluid, electrolyte, and acid-base balance in the newborn period, including dehydration, sodium balance (hyponatraemia and hypernatraemia), hyperkalaemia, interpretation of blood gases (including pH, base excess, and anion gap), respiratory and metabolic acidosis, and hydrops fetalis.
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Archer, Nick, and Nicky Manning. Cardiac function. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199230709.003.0014.

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Assessment 202Treatment 218Cardiac function, if severely compromised, will cause general markers of ill health such as: • Pericardial effusion larger than physiological ( see Table 5.1, p.56).• Hydrops.• Reduced movement.The purpose of the assessments discussed here is to identify the stressed or failing fetal heart at an earlier stage and to provide ways of monitoring changes objectively....
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Publications, ICON Health. Fetal Hydrops: A Medical Dictionary, Bibliography, And Annotated Research Guide To Internet References. Icon Health Publications, 2004.

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Purandare, Amol, and Barbara A. Jantausch. Parvovirus. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190604813.003.0012.

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Parvovirus B19 is a common infection in humans that occurs worldwide. Parvovirus B19 is transmitted through exposure to respiratory droplets, blood, and blood products, and through mother-to-child transmission (MTCT) in utero. Intrauterine parvovirus B19 infection is a rare occurrence during pregnancy but can result in significant morbidity and mortality for the fetus, including severe fetal anemia and nonimmune fetal hydrops (NIFH). Intrauterine transfusion can be successful in treating fetal anemia. Neurodevelopmental impairment has been reported in infants with congenital infection who have
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Chapitres de livres sur le sujet "Hydropsy fetalis"

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Gembruch, Ulrich. "Hydrops fetalis und fetale Anämie." In Ultraschalldiagnostik in Geburtshilfe und Gynäkologie. Springer Berlin Heidelberg, 2025. https://doi.org/10.1007/978-3-662-67373-7_25.

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Schneider, K. T. M., C. v. Kaisenberg, and W. Holzgreve. "Hydrops fetalis." In Manual der fetalen Medizin. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-93551-0_19.

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Park, Joong Shin. "Hydrops fetalis." In Evidence-based Obstetrics and Gynecology. John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781119072980.ch48.

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Chen, Harold. "Hydrops Fetalis." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4614-6430-3_123-2.

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Sel, Görker. "Hydrops Fetalis." In Practical Guide to Oral Exams in Obstetrics and Gynecology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-29669-8_9.

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Huhta, James C. "Hydrops Fetalis." In Visual Guide to Neonatal Cardiology. John Wiley & Sons Ltd, 2018. http://dx.doi.org/10.1002/9781118635520.ch58.

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Benirschke, Kurt, and Peter Kaufmann. "Hydrops Fetalis." In Pathology of the Human Placenta. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4757-4193-3_18.

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Chen, Harold. "Hydrops Fetalis." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-2401-1_123.

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Benirschke, Kurt, Graham J. Burton, and Rebecca N. Baergen. "Erythroblastosis Fetalis and Hydrops Fetalis." In Pathology of the Human Placenta. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23941-0_16.

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Benirschke, Kurt, and Peter Kaufmann. "Erythroblastosis Fetalis and Hydrops Fetalis." In Pathology of the Human Placenta. Springer New York, 1995. http://dx.doi.org/10.1007/978-1-4757-4196-4_16.

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Actes de conférences sur le sujet "Hydropsy fetalis"

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Lau, M., M. Nachtwey, B. Ramsauer, and D. Schlembach. "Management einer Parvovirus-B19 assoziierten fetalen Anämie mit Hydrops fetalis und konsekutiver fetaler Wachstumsretardierung." In 65. Kongress der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe e. V. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1790832.

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Polikarpova, Irina Ivanovna, Elena Anatolyevna Panova, Mikhail Yurievich Petrov, and Evfrosiniya Grigorievna Lyzhina. "CLINICAL CASE OF NON-IMMUNE FETAL HYDROPS IN A NEWBORN CHILD FROM A MOTHER WHO HAD SARS-COV-2 DURING PREGNANCY." In Themed collection of papers from Foreign international scientific conference «Joint innovation - joint development» (Part 3. Biology, medicine, sports) by HNRI «National development» in cooperation with PS of UA. May 2024. - Harbin (China). Crossref, 2024. http://dx.doi.org/10.37539/240530.2024.84.89.034.

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The article describes a clinical case of a newborn with non-immune hydrops fetalis. The well-known etiology of the development of non-immune fetal hydrops is: chromosomal abnormalities, congenital malformations, pathology of the cardiovascular system, pathology of the respiratory system, as well as TORCH infections. Interest in this problem is caused by the low incidence of this disease.
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Reinhardt, K., M. Riemer, E. Wittig, S. Seeger, and M. Tchirikov. "Hydrops fetalis bei schwerer fetaler Anämie aufgrund einer konnatalen Syphilisinfektion." In Kongressabstracts zur 14. Jahrestagung der Mitteldeutschen Gesellschaft für Frauenheilkunde und Geburtshilfe e.V. (MGFG). Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/s-0041-1730840.

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Simon, C., J. Büchel, M. Delius, et al. "Maternales Mirror-Syndrom bei fetalem Hydrops fetalis nach konnataler CMV-Infektion." In Kongressabstracts zur Tagung 2020 der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe (DGGG). © 2020. Thieme. All rights reserved., 2020. http://dx.doi.org/10.1055/s-0040-1718318.

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Pulatova, Gulrux, Rustam Yusupbaev, and Kamola Abdullajonova. "NON-IMMUNE HYDROPS FETALIS – IS CURRENTLY THE PREDOMINANT FORM OF HYDROPS FETALIS." In TENDENZE ATTUALI DELLA MODERNA RICERCA SCIENTIFICA. European Scientific Platform, 2020. http://dx.doi.org/10.36074/05.06.2020.v3.10.

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Becker, WH, M. Hempel, and A. vd Wense. "Nichtimmunologischer Hydrops fetalis bei EPHB4-Mutation." In Interdisziplinärer Kongress | Ultraschall 2018 – 42. Dreiländertreffen SGUM | DEGUM | ÖGUM. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1670384.

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Camara, Rokya, and Katja Schneider. "Chorangiom als Ursache für Hydrops fetalis." In Abstracts zur 49. Jahrestagung der Gesellschaft fär Neonatologie und Pädiatrische Intensivmedizin (GNPI). Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/s-0043-1769361.

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Milera, H., A. Fruth, C. Lindner, et al. "Nicht-immunologischer Hydrops fetalis – eine monozentrische Erfassung." In 29. Deutscher Kongress für Perinatale Medizin. Deutsche Gesellschaft für Perinatale Medizin (DGPM) – „Hinterm Horizont geht's weiter, zusammen sind wir stark“. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3401241.

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Welp, A., I. Fortmann, M. Gembicki, et al. "Infantile Sialinsäurespeicherkrankheit als seltene Ursache des Hydrops fetalis." In 65. Kongress der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe e. V. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1791061.

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Dukatz, R., C. Biele, I. Schönborn, and W. Henrich. "Interdisziplinäres Management bei schwerem fetalem Herzfehler mit Pulmonalatresie, Aortenstenose, VSD, MAPCA und Hydrops fetalis. Ein Case Report." In Interdisziplinärer Kongress | Ultraschall 2019 – 43. Dreiländertreffen DEGUM | ÖGUM | SGUM. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1695982.

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