Literature DB >> 11061079

Renal malformations in children with Turner's syndrome.

P Chang1, Y K Tsau, W Y Tsai, W S Tsai, J W Hou, P H Hsiao, J S Lee.   

Abstract

Between 1988 and 1999, renal sonography and intravenous urography were performed to detect renal malformations in 54 patients with Turner's syndrome (TS). The mean age of these patients at diagnosis of TS was 9.2 +/- 4.6 years. Renal malformations were detected in 21 patients by intravenous urography and there was no significant difference in the frequency of renal malformations among different karyotype groups. Horseshoe kidney was the most common renal malformation, followed by duplex kidney. Fifteen of 21 renal malformations were not detected by renal sonography. We conclude that these TS patients had a high frequency of renal malformations, and that the detection rate of horseshoe kidney and duplex kidney by renal sonography was not satisfactory. Although renal sonography alone can be used to detect more severe renal malformations that may need further management, it may underestimate the frequency of renal malformation in children with TS.

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Year:  2000        PMID: 11061079

Source DB:  PubMed          Journal:  J Formos Med Assoc        ISSN: 0929-6646            Impact factor:   3.282


  7 in total

1.  Renal morphology and function from childhood to adulthood in Turner syndrome.

Authors:  Tetsushi Ogawa; Fumihiko Takizawa; Yuri Mukoyama; Atsushi Ogawa; Junko Ito
Journal:  Clin Exp Nephrol       Date:  2021-02-22       Impact factor: 2.801

2.  Main Physical Features, Echocardiographic and Renal Ultrasonographic Findings of Turner Syndrome in 107 Pediatric Patients.

Authors:  Akçahan Akalın; İlker Ertuğrul; Pelin Özlem Şimşek-Kiper; Gülen Eda Utine; Koray Boduroğlu
Journal:  Mol Syndromol       Date:  2021-08-12

3.  An extremely rare case of unilateral renal arterial and venous multiple deformity, combined with duplex pelvis and malrotation.

Authors:  Liang Gao; Siyuan Bu; Fan Wan; Fei Zhao; Qiang Wei; Ping Han; Tianyong Fan; Lu Yang
Journal:  Int Urol Nephrol       Date:  2013-02-01       Impact factor: 2.370

4.  Turner Syndrome Genotype and phenotype and their effect on presenting features and timing of Diagnosis.

Authors:  I Al Alwan; Khadora M; Nasrat G; Omair A; Brown L; Al Dubayee M; Badri M
Journal:  Int J Health Sci (Qassim)       Date:  2014-04

5.  Turner syndrome and associated problems in Turkish children: a multicenter study.

Authors:  Ediz Yeşilkaya; Abdullah Bereket; Feyza Darendeliler; Firdevs Baş; Şükran Poyrazoğlu; Banu Küçükemre Aydın; Şükran Darcan; Bumin Dündar; Muammer Büyükinan; Cengiz Kara; Erkan Sarı; Erdal Adal; Ayşehan Akıncı; Mehmet Emre Atabek; Fatma Demirel; Nurullah Çelik; Behzat Özkan; Bayram Özhan; Zerrin Orbak; Betül Ersoy; Murat Doğan; Ali Ataş; Serap Turan; Damla Gökşen; Ömer Tarım; Bilgin Yüksel; Oya Ercan; Şükrü Hatun; Enver Şimşek; Ayşenur Ökten; Ayhan Abacı; Hakan Döneray; Mehmet Nuri Özbek; Mehmet Keskin; Hasan Önal; Nesibe Akyürek; Kezban Bulan; Derya Tepe; Hamdi Cihan Emeksiz; Korcan Demir; Deniz Kızılay; Ali Kemal Topaloğlu; Erdal Eren; Samim Özen; Saygın Abalı; Leyla Akın; Beray Selver Eklioğlu; Sultan Kaba; Ahmet Anık; Serpil Baş; Tolga Ünüvar; Halil Sağlam; Semih Bolu; Tolga Özgen; Durmuş Doğan; Esra Deniz Çakır; Yaşar Şen; Nesibe Andıran; Filiz Çizmecioğlu; Olcay Evliyaoğlu; Gülay Karagüzel; Özgür Pirgon; Gönül Çatlı; Hatice Dilek Can; Fatih Gürbüz; Çiğdem Binay; Veysel Nijat Baş; Kürşat Fidancı; Adem Polat; Davut Gül; Cengizhan Açıkel; Hüseyin Demirbilek; Peyami Cinaz; Carolyn Bondy
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-03

6.  Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features

Authors:  Nataliya Zelinska; Iryna Shevchenko; Evgenia Globa
Journal:  J Clin Res Pediatr Endocrinol       Date:  2018-02-28

7.  DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.

Authors:  Amit Sharma; Muhammad Ahmer Jamil; Nicole Nuesgen; Felix Schreiner; Lutz Priebe; Per Hoffmann; Stefan Herns; Markus M Nöthen; Holger Fröhlich; Johannes Oldenburg; Joachim Woelfle; Osman El-Maarri
Journal:  Clin Epigenetics       Date:  2015-07-28       Impact factor: 6.551

  7 in total

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