Literature DB >> 2274490

First and early second-trimester diagnosis of fetal urinary tract anomalies using transvaginal sonography.

M Bronshtein1, N Yoffe, J M Brandes, Z Blumenfeld.   

Abstract

Urinary tract anomalies are common. Prenatal diagnosis is important and enables either special obstetric management or termination of pregnancy and probably in the future, intrauterine intervention. Transvaginal sonography (TVS) allows visualization of the normal and anomalous fetal urinary tract at an early stage. One thousand nine hundred and forty women were examined via TVS at an early stage of pregnancy between 10 and 16 weeks from the last menstrual period (LMP) and 35 anomalies (1.8 per cent) were clearly identified: 29 cases of low urinary tract obstruction, 2 cases of multicystic dysplastic kidney, 2 cases of polycystic kidney (infantile type), 1 case of double collecting system, and 1 case of horseshoe kidney. Potter syndrome could be ruled out in three patients who had delivered fetuses suffering from this anomaly in previous pregnancies. The concise and early identification of anomalies makes TVS an important aid in the hands of the obstetrician, ultrasonographer, and neonatologist.

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Year:  1990        PMID: 2274490     DOI: 10.1002/pd.1970101005

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  4 in total

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Authors:  J Radhakrishnan; G Lievano
Journal:  Indian J Pediatr       Date:  1997 May-Jun       Impact factor: 1.967

Review 2.  First trimester ultrasound: current approaches and practical pitfalls.

Authors:  Ozgur Oztekin
Journal:  J Med Ultrason (2001)       Date:  2009-08-25       Impact factor: 1.314

3.  Complementary role of magnetic resonance imaging after ultrasound examination in assessing fetal renal agenesis: a case report.

Authors:  Tomasz Gęca; Arkadiusz Krzyżanowski; Aleksandra Stupak; Anna Kwaśniewska; Tomasz Pikuła; Radosław Pietura
Journal:  J Med Case Rep       Date:  2014-03-12

4.  Two novel deleterious variants of Angiotensin-I-converting Enzyme gene identified in a family with recurrent anhydramnios.

Authors:  Jingwei Wang; Qiao Bin; Biheng Cheng; Li Yan; Liang Xiong; Bi-Hua Tan; Mary McGrath; Gayle M Smink; Chunhua Song; Yongqing Tong
Journal:  Mol Genet Genomic Med       Date:  2020-04-23       Impact factor: 2.183

  4 in total

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