نتایج جستجو برای: hydrops fetalis

تعداد نتایج: 1807  

Journal: :The Journal of the American Board of Family Practice 2003
Jin Xu Thomas C Raff Nabil S Muallem A George Neubert

BACKGROUND Fetal infection by human parvovirus B19 is a common cause of fetal anemia, nonimmune hydrops fetalis, and spontaneous abortion and can result in fetal death. Recent improvements in diagnosing parvovirus infections and the availability of intrauterine transfusion have reduced the overall rate of fetal loss after maternal exposure. METHODS We report two cases of maternal parvovirus i...

Journal: :Journal of clinical microbiology 1999
M Musiani P Pasini M Zerbini G Gentilomi A Roda G Gallinella E Manaresi S Venturoli

Parvovirus B19 can be transmitted transplacentally from the infected mother to the fetus during pregnancy, and hydrops fetalis, abortion, or stillbirth can result. In our study we explored the use of chemiluminescence in situ hybridization to detect B19 DNA on cord blood cells, amniotic fluid cells, and pleuric fluid cells from several cases of hydrops fetalis. B19 DNA was detected by using dig...

2016
Seyfettin Uludağ

A case with a pleural effusion and hydrops fetalis has been presented. Good outcome had been achieved by a single thoracentesis and a healthy baby w as delivered at the 39th w eek of pregnancy. In a fetus with a pleural effusion and hydrops fetalis, normal like echogenic view of the affected side lung and lung expansion during aspiration without any signs of fetal distress are good prognostic s...

Journal: :Journal of clinical pathology 1993
J Nelson B Kenny D O'Hara A Harper D Broadhead

Mucopolysaccharidosis type VII (MPS VII, beta glucuronidase deficiency) has been described in association with non-immune hydrops fetalis. Three consecutive pregnancies in an itinerant family, which resulted in stillbirths caused by non-immune hydrops are described. The parents were closely related and there was a strong family history of storage disorders. The main clue to the diagnosis, howev...

2014
Wassim A. Hassan Shyam Das Daniel Thompson

α-Thalassaemia is the most common inherited disorder of Haemoglobin (Hb) production in southeast Asia, resulting from deficient synthesis of the α-globin chain component of the haemoglobin molecule due to deletion or inactivation of one or more of the normal four alpha-chain genes. The severity of the condition depends on the number of genes inactivated. The severest form is Hb Barts hydrops fe...

Journal: :Archives of Disease in Childhood 1988

Journal: :Journal of Perinatal Medicine 1982

Journal: :The Ulster Medical Journal 1990
D. C. Wilson H. L. Halliday G. McClure M. M. Reid

Fetal hydrops (hydrops fetalis) remains a significant cause of fetal and neonatal mortality. The decreased incidence of rhesus iso-immunisation due to prophylaxis with rhesus immune globulin (anti-D), improved antenatal ultrasound screening, and advances in neonatal intensive care have greatly altered the clinical outlook in this condition. A retrospective review of all 27 liveborn cases of hyd...

Journal: :Journal of Pediatric Nursing 2017

Journal: :Case Reports in Obstetrics and Gynecology 2014

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