Literature DB >> 1481851

Urinary tract involvement in EEC syndrome: a clinical study in 25 Brazilian patients.

A C Nardi1, U Ferreira, N R Netto Júnior, L A Magna, E S Rodini, A Richieri-Costa.   

Abstract

We have evaluated 25 patients (14 isolated and 11 familial cases) with the EEC syndrome for genitourinary (GU) tract anomalies through intravenous pyelogram (IVP), voiding urethrocystography, and sonographic examination. Fifty-two percent of the patients (7 isolated and 6 familial cases) had involvement of the urinary tract, with no significant difference between isolated and familial cases. The present data seem to reflect the best estimate of the prevalence of genitourinary anomalies in patients with the EEC syndrome.

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Year:  1992        PMID: 1481851     DOI: 10.1002/ajmg.1320440617

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

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Authors:  Nihal Hatipoğlu; Selim Kurtoğlu; Derya Büyükayhan; Mustafa Akçakuş
Journal:  J Clin Res Pediatr Endocrinol       Date:  2009-08-08

2.  Familial clustering of a rare syndrome.

Authors:  Jayashree Nadkarni; Hari Ganesh; Rashmi Dwivedi
Journal:  Indian J Hum Genet       Date:  2011-01

3.  TP63-mutation as a cause of prenatal lethal multicystic dysplastic kidneys.

Authors:  Isabel Friedmann; Carla Campagnolo; Nancy Chan; Ghislain Hardy; Maha Saleh
Journal:  Mol Genet Genomic Med       Date:  2020-09-02       Impact factor: 2.183

  3 in total

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