Prenatal Diagnosis of Bartter Syndrome with Biochemical Examination of Amniotic Fluid: Case Report

2007 ◽  
Vol 22 (3) ◽  
pp. 206-208 ◽  
Author(s):  
Banu Dane ◽  
Murat Yayla ◽  
Cem Dane ◽  
Ahmet Cetin
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Amniotic Fluid ◽  
Bartter Syndrome ◽  
Biochemical Examination

scholarly journals Biochemical examination of mother’s urine is useful for prenatal diagnosis of Bartter syndrome

1999 ◽  
Vol 19 (7) ◽  
pp. 671-673 ◽  
Author(s):  
Yuriko Matsushita ◽  
Yoshikatsu Suzuki ◽  
Naomi Oya ◽  
Shoji Kajiura ◽  
Kazuki Okajima ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Bartter Syndrome ◽  
Biochemical Examination

scholarly journals Bartter Syndrome Prenatal Diagnosis Based on Amniotic Fluid Biochemical Analysis

2010 ◽  
Vol 67 (3) ◽  
pp. 300-303 ◽  
Author(s):  
Arnaud Garnier ◽  
Sophie Dreux ◽  
Rosa Vargas-Poussou ◽  
Jean-François Oury ◽  
Alexandra Benachi ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Amniotic Fluid ◽  
Biochemical Analysis ◽  
Bartter Syndrome

Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone

2015 ◽  
Vol 36 (1) ◽  
pp. 88-91
Author(s):  
Myriam L. Rachid ◽  
Sophie Dreux ◽  
Gauthier Pean de Ponfilly ◽  
Rosa Vargas-Poussou ◽  
Isabelle Czerkiewicz ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Amniotic Fluid ◽  
Bartter Syndrome

scholarly journals Prenatal diagnosis of megaduodenum using ultrasound: a case report

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Kaihui Zeng ◽  
Dongmei Li ◽  
Yao Zhang ◽  
Chengcheng Cao ◽  
Ruobing Bai ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Amniotic Fluid ◽  
Ultrasound Examination ◽  
Cystic Mass ◽  
Developmental Defect ◽  
Case Presentation ◽  
Amniotic Fluid Volume ◽  
Cystic Masses

Abstract Background Congenital megaduodenum is a rare disorder; however, its prenatal diagnosis has not been reported previously. We report the case of an abdominal cystic mass in a fetus that was later diagnosed as megaduodenum. Case presentation An abdominal cystic mass was found during ultrasonography of a fetus at 11 weeks of gestation. The mass progressively enlarged with gestation. The amniotic fluid volume decreased and then returned to normal. During the last prenatal ultrasound examination, the mass was observed communicating with the stomach; therefore, duodenal dilation was suspected. Finally, the patient was diagnosed with megaduodenum caused by a developmental defect in the nerve plexus. Conclusions Congenital megaduodenum is a differential diagnosis of massive fetal abdominal cystic masses. Ultrasound examinations of such masses communicating with the stomach may help determine the diagnosis.

Prenatal diagnosis of Bartter syndrome: amniotic fluid aldosterone

2017 ◽  
Vol 75 (2) ◽  
pp. 204-208
Author(s):  
Myriam Rachid ◽  
Sophie Dreux ◽  
Gauthier Pean de Ponfilly ◽  
Rosa Vargas-Poussou ◽  
Isabelle Czerkiewicz ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Amniotic Fluid ◽  
Bartter Syndrome

A rare case of epignatus in the fetus

2017 ◽  
Author(s):  
N.V. Mashinets, V.N. Demidov, Y.L. Podurovskaya et all
Keyword(s):  
Blood Flow ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Surgical Treatment ◽  
Amniotic Fluid ◽  
Histological Examination ◽  
Tumor Size ◽  
Rare Case ◽  
Review Of The Literature ◽  
Positive Effect

We present a review of the literature and own case report of prenatal diagnosis of epignatus at 31 week of gestation. Ultrasound of the fetus revealed a massive formation of solid structure of the blubber of the mouth. The size of epignatus was 3,0  3,0  2,8 cm, intratumoral blood flow was not determined, the amount of amniotic fluid was normal. With the progression of pregnancy the tumor size has not increased. After the birth the neonate was an independent breath. Carried out surgical treatment with a positive effect. The diagnosis of epignatus confirmed by histological examination.

scholarly journals Prenatal diagnosis of granular cell myoblastoma: A case report

2006 ◽  
Vol 59 (11-12) ◽  
pp. 573-576
Author(s):  
Aleksandra Novakov-Mikic ◽  
Ljiljana Ivanovic ◽  
Milos Lucic ◽  
Aleksandar Kiralj ◽  
Katarina Koprivsek ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Oral Cavity ◽  
Cesarean Section ◽  
Amniotic Fluid ◽  
Granular Cell ◽  
Histopathological Diagnosis ◽  
Normal Female ◽  
Granular Cell Myoblastoma

Introduction. The aim of this paper is to present a case of prenatal diagnosis of a congenital tumor of the oral cavity diagnosed at 28 weeks of gestation. Case report. After the diagnosis of oral cavity tumor was made by 2D ultrasound, a 3D scan was performed, which confirmed the diagnosis revealing a peduncle at the upper border of maxilla. A detailed scan was performed and no additional anomalies were seen. Magnetic resonance imaging was performed, confirming the diagnosis and the site of the tumor. Karyotype was previously done, and a normal female karyotype was found. Regular three-week follow-up scans were performed to follow the growth of the tumor, as well as the state of the amniotic fluid. No tumor growth was detected, and the amniotic fluid volume was normal until 39 weeks of gestation. Cesarean section was scheduled, due to the risk of tumor disruption during a vaginal delivery. A maxillofacial surgeon was present during an uneventful cesarean section and a complete surgical excision was done immediately after the baby was extracted and umbilical cord ligated. The histopathological diagnosis was: granular cell myoblastoma. The female newborn was developing normally, and at 5 months of age there were no traces of scarring at the place of the tumor. Conclusion. In cases of prenatal diagnosis of tumors of the oral cavity, where development of polyhydramnios can be expected, as well as difficulties with feeding and breathing after birth, it is important to make a plan for adequate follow-up and prompt surgical treatment immediately after birth. .

Prenatal diagnosis of an epignathus associated with a 49, XXXXY karyotype – a case report

2007 ◽  
Vol 28 (S 1) ◽  
Author(s):  
I Staboulidou ◽  
K Miller ◽  
G Göhring ◽  
P Hillemanns ◽  
M Wüstemann
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis
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