Literature DB >> 9021589

Multicystic kidney in siblings.

M S Moazin1, S Ahmed, K Fouda-Neel.   

Abstract

Two siblings (one girl and one boy), with a left multicystic kidney in whom a renal abnormality had been recognized prenatally, are reported. A large renal mass was present in both patients and the second sibling also had hypertension. Early surgical resection was carried out with satisfactory clinical progress and resolution of the hypertension. Multicystic kidney is considered a developmental abnormality with a sporadic incidence. These cases and other reports of familial incidence in the literature indicate that there may also be a genetic basis for the abnormality.

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Year:  1997        PMID: 9021589     DOI: 10.1016/s0022-3468(97)90114-7

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  3 in total

1.  Familial multicystic dysplastic kidney.

Authors:  Toru Watanabe; Akira Yamazaki; Takumi Kurabayashi; Jin-ichi Hanaoka
Journal:  Pediatr Nephrol       Date:  2005-05-24       Impact factor: 3.714

2.  Unilateral multicystic dysplastic kidney: single-center experience.

Authors:  Aysel Kiyak; Alev Yilmaz; Pinar Turhan; Serdar Sander; Gulay Aydin; Gonul Aydogan
Journal:  Pediatr Nephrol       Date:  2008-08-12       Impact factor: 3.714

Review 3.  The diagnostic value of ultrasound in cystic kidney diseases.

Authors:  Udo Vester; Birgitta Kranz; Peter F Hoyer
Journal:  Pediatr Nephrol       Date:  2008-09-23       Impact factor: 3.714

  3 in total

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