Volume 44, Issue 6 pp. 803-806
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Urinary tract involvement in EEC syndrome: A clinical study in 25 Brazilian patients

Aguinaldo C. Nardi

Aguinaldo C. Nardi

Serviço de Genética Clínica, Universidade Estadual de Campinas, Campinas, Brazil

Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Bauru and Division of Urology, Universidade Estadual de Campinas, Campinas, Brazil

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Ubirajara Ferreira

Ubirajara Ferreira

Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Bauru and Division of Urology, Universidade Estadual de Campinas, Campinas, Brazil

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Nelson Rodrigues Netto Jr.

Nelson Rodrigues Netto Jr.

Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Bauru and Division of Urology, Universidade Estadual de Campinas, Campinas, Brazil

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Luis Alberto Magna

Luis Alberto Magna

Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Bauru and Division of Urology, Universidade Estadual de Campinas, Campinas, Brazil

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E. S. O. Rodini

E. S. O. Rodini

Serviço de Genética Clínica, Universidade Estadual de Campinas, Campinas, Brazil

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A. Richieri-Costa

Corresponding Author

A. Richieri-Costa

Serviço de Genética Clínica, Universidade Estadual de Campinas, Campinas, Brazil

Serviço de Genética Clínica, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, P.O. Box 620, 17043 Bauru, SP, BrazilSearch for more papers by this author
First published: 1 December 1992
Citations: 21

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. © 1992 Wiley-Liss, Inc.

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