Literature DB >> 2204162

Prenatal diagnosis by ultrasound in pregnancies at risk for autosomal recessive polycystic kidney disease.

A Reuss1, J W Wladimiroff, P A Stewart, M F Niermeijer.   

Abstract

In 15 pregnancies at risk of the autosomal recessive type of polycystic kidney disease (ARPKD), there were six recurrences (40%), five of which were diagnosed prenatally between 17 and 26 weeks (mean, 22 weeks). In the remaining affected case, normal kidney size and echogenicity were still present at 30 weeks of gestation. Fetal kidney enlargement and increased echogenicity are the key ultrasonographic signs for the detection of ARPKD. Absent fetal bladder filling and oligohydramnios were only documented in two of the six affected pregnancies. The variability in onset, the intrafamilial variability and the limitations of excluding ARPKD by second trimester ultrasound have to be considered when counselling a couple at risk for this particular disorder.

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Year:  1990        PMID: 2204162     DOI: 10.1016/0301-5629(90)90065-k

Source DB:  PubMed          Journal:  Ultrasound Med Biol        ISSN: 0301-5629            Impact factor:   2.998


  7 in total

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Review 2.  Diagnosis and management of childhood polycystic kidney disease.

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3.  Fetal imaging prompts maternal diagnosis: autosomal dominant polycystic kidney disease.

Authors:  A G Euser; J F Sung; S Reeves
Journal:  J Perinatol       Date:  2015-07       Impact factor: 2.521

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5.  Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway.

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Review 6.  Perinatal assessment of hereditary cystic renal diseases: the contribution of sonography.

Authors:  Fred E Avni; Laurent Garel; Marie Cassart; Anne Massez; Daniele Eurin; François Didier; Michelle Hall; Rita L Teele
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7.  Cost-effective PKHD1 genetic testing for autosomal recessive polycystic kidney disease.

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  7 in total

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