Idiopathic Polyhydramnios and Postnatal Abnormalities

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منابع مشابه

Idiopathic polyhydramnios and postnatal abnormalities.

OBJECTIVE To investigate the proportion and type of fetal anomalies that are associated with polyhydramnios and to examine whether in cases with idiopathic polyhydramnios during the course of pregnancy and fetal anomalies only diagnosed after birth, antenatal characteristics differ. METHODS This was a retrospective study involving all pregnancies with polyhydramnios defined by a deepest pool ...

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Perinatal Outcome in Idiopathic Polyhydramnios.

OBJECTIVES To study perinatal outcome in idiopathic polyhydramnios. METHODS Case-control study was conducted in 500 pregnant women with idiopathic polyhydramnios (study group) and 500 normal pregnant women (control group) attending the outpatient department of SHKM Medical College, Haryana. Perinatal outcomes were recorded in both the groups. RESULTS Out of 500 cases with idiopathic polyhyd...

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Idiopathic Recurrent Polyhydramnios: A Rare Case Report

Polyhydramnios occurs in 1-2% of pregnancies and may be idiopathic in more than half of the cases. The diagnosis of idiopathic polyhydramnios can be made only in the absence of maternal diabetes, fetal anomalies, aneuploidies, multiple gestation, Rh incompatibility, placental tumours and non-immune hydrops. Rarely, idiopathic polyhydramnios may be recurrent in future pregnancies and sometimes n...

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Perinatal Outcomes of Idiopathic Polyhydramnios with Normal Ultrasound: A Systematic Review and Meta-Analysis

Background: Incidence of polyhydramnios in various studies has been reported from 0.2 to 3.9%. Approximately, 50-60% of cases are idiopathic with no known etiology. We aimed to investigate perinatal outcomes of idiopathic polyhydramnios with a normal ultrasound. Materials and Methods: In this study, Persian and English databases including Barakatkns, SID, Magiran, Medline, Science Direct, Scopu...

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"Idiopathic" mental retardation and new chromosomal abnormalities

Mental retardation is a heterogeneous condition, affecting 1-3% of general population. In the last few years, several emerging clinical entities have been described, due to the advent of newest genetic techniques, such as array Comparative Genomic Hybridization. The detection of cryptic microdeletion/microduplication abnormalities has allowed genotype-phenotype correlations, delineating recogni...

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ژورنال

عنوان ژورنال: Fetal Diagnosis and Therapy

سال: 2012

ISSN: 1421-9964,1015-3837

DOI: 10.1159/000338659