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Dive into the research topics where Amira Egic is active.

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Featured researches published by Amira Egic.


Fetal Diagnosis and Therapy | 2009

Intrauterine treatment of large fetal neck lymphangioma with OK-432.

Zeljko Mikovic; Radoje Simic; Amira Egic; Tatjana Stosic Opincal; Katarina Koprivsek; Dusan Stanojevic; Mirjana Bogavac; Mirjana Popovac; Vesna Mandic

Lymphangiomas are benign vascular malformations of the lymphatic system and most commonly present in the neck area. Large lymphangiomas may compress and/or displace the larynx, trachea and esophagus and cause serious respiratory and feeding problems in neonates. Prenatal therapy could eliminate the risks of the mentioned complications. Prenatal therapy may include the EXIT (ex utero intrapartum treatment) procedure. As this procedure has certain risks for both the neonate and mother, the introduction of a safer method is justified. The use of OK-432, as a sclerosing agent, has shown positive results in several published cases of cystic hygroma, but there is no study about the prenatal use of this agent in the treatment of lymphangioma. The aim of this study was to present our experience with intrauterine intralesional injection of OK-432 in the treatment of neck lymphangiomas. Two cases of large multicystic neck lymphangiomas that were closely situated to the fetal airway were treated by single intralesional injection of OK-432. We noticed a progressive decrease in tumor volume throughout gestation. We did not experience any complications and there were no respiratory or feeding problems in the neonates. The esthetical appearance was satisfactory and both children were normal at the age of 2 years and 6 months, respectively. This report suggests that prenatal intralesional injection of OK-432 might be a safe and effective treatment in selected cases with large fetal neck lymphangiomas.


Prenatal Diagnosis | 2012

Improved diagnostic accuracy by using secondary ultrasound markers in the first-trimester screening for trisomies 21, 18 and 13 and Turner syndrome

Natasa Karadzov-Orlic; Amira Egic; Zagorka Milovanovic; Maja Marinkovic; Barbara Damnjanovic-Pazin; Relja Lukic; Ivana Joksic; Aleksandar Ćurković; Zeljko Mikovic

The aim of this study was to examine the effectiveness of a combination of parameters at first‐trimester screening for fetal aneuploidies, including ultrasound assessment of the nasal bone (NB), blood flow in the ductus venosus (DV) and flow across the tricuspid valve.


Obstetrics and Gynecology International | 2014

Degree and rate of growth discordance in dichorionic twins conceived by in vitro fertilization.

Amira Egic; Donka Mojovic; Zagorka Milovanovic; Aleksandar B. Jurisic; Ljubomir P. Srbinovic; Suzana P. Krsmanovic; Natasa Karadzov-Orlic

Objective. Our objective was to estimate degree and rate of discordant growth and its impact on perinatal outcome in dichorionic twin pregnancies conceived by in vitro fertilization (IVF) compared to those conceived spontaneously. Study Design. Growth discordance was defined as 90th percentiles for the study population. Adverse perinatal outcome was defined as 5-minute Apgar score <7 and/or admission to neonatal intensive care unit. Results. In the total study population of dichorionic twins (176 conceived by IVF and 215 spontaneously), 30% discordant growth represented the 90th percentile. After adjusting for gestational age, discordant twins conceived by IVF or spontaneously were at higher risk for adverse perinatal outcome (hazard ratio 4.4; 95% CI 2.4–8.3, P < 0.0001; hazard ratio 2.5; 95% CI 1.5–4.4, P = 0.001, resp.). Similar rates of 5-minute Apgar score <7, admission to neonatal intensive care unit, and delivery <34 weeks were found between discordant twins conceived by IVF and those conceived spontaneously. Conclusion. Dichorionic twins conceived by IVF are at similar risk for the rate and degree of discordant growth and adverse perinatal outcome compared to dichorionic twins conceived spontaneously.


Srpski Arhiv Za Celokupno Lekarstvo | 2011

[Multifoetal pregnancies complicated by reversed arterial perfusion: report of four cases].

Zeljko Mikovic; Natasa Karadzov-Orlic; Maja Marinkovic; Slavisa Djuricic; Amira Egic; Vladimir Pazin; Mirjana Popovac; Dijana Smolovic

INTRODUCTION Twin reversed arterial perfusion syndrome (TRAP) or acardiac anomaly presents a rare and severe complication affecting monochorionic multiple pregnancies occurring in 1 per 35,000 pregnancies or 1 per 100 of monozygotic twins. We report four cases of multiple pregnancies with TRAP diagnosed over the last 2 years, which were under check-up and treatment during the entire pregnancy course finalized by delivery. OUTLINE OF CASES In two cases pregnancies were trigeminal, and other two geminal, with acardia of one foetus, by anceps type in three and acephalus in one. Expectant management was initially done in all cases. The relation of acardiac and donor abdominal circumference was below 50% and negative signs of the donors cardiac failure were detected in two cases, so that expectative management was continued until delivery. Due to obstetric indications, a cesarean section was performed on the 33rd and 34th gestational week, and healthy newborns were delivered. Another two acardiac twins had abdominal circumference ratio between the acardiac fetus and the donor of over 50%, and signs of congestive heart failure in the donor, which indicated invasive therapeutic procedure with absolute alcohol chemisclerosis; it was done by alcohol injection into the acardiac abdominal aorta which interrupted the retrograde blood-flow into the acardiac umbilicus. In the first case a successful intervention was performed at 29th gestational week, but after 12 hours distress signs were registered. The delivery was finalized by a cesarean section, and a live donor was delivered. In the second case the intervention was successfully done at the 20th gestational week, and after 96 hours from the intervention lethal ending of the donor was registered. CONCLUSION Bearing in mind that the occurrence of TRAP is rare, it is necessary to sum-up experiences from a larger number of centres to determine efficient therapeutic procedure.


Srpski Arhiv Za Celokupno Lekarstvo | 2011

Prenatal diagnosis of meconium ileus and meconium peritonitis: Indications for cystic fibrosis testing

Amira Egic; Zeljko Mikovic; Vesna Mandic; Natasa Karadzov

INTRODUCTION More recently, the regions of increased abdominal echogenicity such as echogenic bowel, meconium ileus and meconium peritonitis have been associated with an increased prevalence of a variety of unfavourable outcomes including chromosomal abnormalities, cytomegalovirus infection, intestinal obstruction, anorectal malformations and cystic fibrosis. Earlier prenatal examinations of these severe autosomal recessive diseases had been suggested only to families with history of cystic fibrosis. Recently, systemic examination has been introduced by ultrasound with bowel hyperechogenicity where the fetus is the index case for genetic disease. Risk for cystic fibrosis with this ultrasonography findings ranges from 0-33%. OUTLINE OF CASES Two patients are presented, aged 24 and 29 years, both primigravide. The first one had ultrasonography finding of meconium peritonitis revealed at the 37th week of gestation and the other meconium ileus revealed on ultrasonography at the 29th week of gestation. Both patients had prenatal testing of foetal blood obtained by cordocenthesis, both had normal kariotype and were negative for cytomegalovirus infection. Parental DNA testing for the 2nd patient showed that parents were not carriers for the 29 most frequent mutations. Both neonates had intestinal obstruction, underwent surgery and early postoperative course was normal. Hystopathological finding suggested a possibility of cystic fibrosis for the 1st patient, but parents did not want to be tested and for the 2nd one congenital bowel stenosis as a cause of intestinal obstruction. CONCLUSION Ultrasonographic echogenic bowel is an indication for invasive procedures for foetal blood testing for chromosomal abnormalities, congenital infections and parental testing for cystic fibrosis. Only if parental heterozygosity is proven foetus should be tested.


Reproductive Toxicology | 2017

Increased oxidative stress and cytokinesis-block micronucleus cytome assay parameters in pregnant women with gestational diabetes mellitus and gestational arterial hypertension

Mina Toljic; Amira Egic; Jelena Munjas; Natasa Karadzov Orlic; Zagorka Milovanovic; Aleksandra Radenkovic; Jovana Vuceljic; Ivana Joksic


Srpski Arhiv Za Celokupno Lekarstvo | 2003

A longitudinal analysis of arterial dopler parameters in growth restricted fetuses

Zeljko Mikovic; Vesna Mandic; Milan Djukic; Amira Egic; Dejan Filimonovic; Nikola Cerovic; Mirjana Popovac


Prenatal Diagnosis | 2015

Screening performances of abnormal first-trimester ductus venosus blood flow and increased nuchal translucency thickness in detection of major heart defects.

Natasa Karadzov-Orlic; Amira Egic; Dejan Filimonovic; Barbara Damnjanovic-Pazin; Zagorka Milovanovic; Relja Lukic; Vesna Mandic; Ivana Joksic; Vladimir Vukomanović; Jovan Kosutic; Slavisa Djuricic; Zeljko Mikovic


Srpski Arhiv Za Celokupno Lekarstvo | 2005

Birth weight discordance and perinatal mortality among triplets

Amira Egic; Zeljko Mikovic; Dejan Filimonovic; Anka Cirovic


Srpski Arhiv Za Celokupno Lekarstvo | 2012

Screening for aneuploidies by maternal age, fetal nuchal translucency and maternal serum biochemistry at 11-13+6 gestational weeks.

Natasa Karadzov-Orlic; Amira Egic; Dejan Filimonovic; Maja Marinkovic; Barbara Damnjanovic-Pazin; Zagorka Milovanovic; Ivana Joksic; Snezana Brankovic; Relja Lukic; Vesna Mandic; Nikola Cerovic; Donka Mojovic; Sanja Plamenac; Minja Stankovic; Dragana Maglić; Zeljko Mikovic

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Relja Lukic

University of Belgrade

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