Literature DB >> 15973528

A familial case of multicystic dysplastic kidney.

Takashi Sekine1, Yoshiyuki Namai, Atsuhiro Yanagisawa, Hiroshi Shirahama, Yukie Tashiro, Masahito Terahara, Michio Nagata, Yutaka Harita, Utako Fukuoka, Jun Inatomi, Takashi Igarashi.   

Abstract

A familial case of multicystic dysplastic kidney (MCDK) is described. The proband is a one-year-old boy with left MCDK, and his father was also revealed to have unilateral MCDK. The mother had two abortions; the second pregnancy was terminated because of bilateral MCDK of the fetus (Potter anomaly). The two patients and the aborted male fetus did not have any malformations except for MCDK. Thus in this family MCDK occurs as an isolated phenomenon in three individuals within two generations, presumably as a result of autosomal dominant inheritance.

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Year:  2005        PMID： 15973528     DOI： 10.1007/s00467-005-1905-x

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


  17 in total

1.  Autosomal dominant inheritance of multicystic dysplastic kidney.

Authors:  T Srivastava; R E Garola; S Hellerstein
Journal:  Pediatr Nephrol       Date:  1999-08       Impact factor: 3.714

2.  Insulin-like growth factor (IGF) and IGF binding protein gene expression in multicystic renal dysplasia.

Authors:  D G Matsell; T Bennett; R A Armstrong; P Goodyer; C Goodyer; V K Han
Journal:  J Am Soc Nephrol       Date:  1997-01       Impact factor: 10.121

3.  Initial pathological events in renal dysplasia with urinary tract obstruction in utero.

Authors:  S Shibata; M Shigeta; Y Shu; T Watanabe; M Nagata
Journal:  Virchows Arch       Date:  2001-10       Impact factor: 4.064

4.  Hereditary renal adysplasia in a three generations family.

Authors:  B Doray; B Gasser; I Reinartz; C Stoll
Journal:  Genet Couns       Date:  1999

Review 5.  Pax2 in development and renal disease.

Authors:  G R Dressler; A S Woolf
Journal:  Int J Dev Biol       Date:  1999       Impact factor: 2.203

Review 6.  Antenatal diagnosis of Multicystic Renal Dysplasia.

Authors:  A Ranke; M Schmitt; F Didier; P Droulle
Journal:  Eur J Pediatr Surg       Date:  2001-08       Impact factor: 2.191

7.  A family study and the natural history of prenatally detected unilateral multicystic dysplastic kidney.

Authors:  R A Belk; D F M Thomas; R F Mueller; P Godbole; A F Markham; M J Weston
Journal:  J Urol       Date:  2002-02       Impact factor: 7.450

8.  The PAX2 tanscription factor is expressed in cystic and hyperproliferative dysplastic epithelia in human kidney malformations.

Authors:  P J Winyard; R A Risdon; V R Sams; G R Dressler; A S Woolf
Journal:  J Clin Invest       Date:  1996-07-15       Impact factor: 14.808

Review 9.  The role of PAX2 in normal and abnormal development of the urinary tract.

Authors:  M R Eccles
Journal:  Pediatr Nephrol       Date:  1998-11       Impact factor: 3.714

10.  Hereditary renal adysplasia: new observations and hypotheses.

Authors:  P Moerman; J P Fryns; S H Sastrowijoto; K Vandenberghe; J M Lauweryns
Journal:  Pediatr Pathol       Date:  1994 May-Jun
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  3 in total

1.  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 2.  Are therapeutic stem cells justified in bilateral multicystic kidney disease? A review of literature with insights into the embryology.

Authors:  Shilpa Sharma; Devendra K Gupta; Lalit Kumar; A K Dinda; A Bagga; S Mohanty
Journal:  Pediatr Surg Int       Date:  2007-06-14       Impact factor: 1.827

3.  [Prenatal diagnosis of multicystic dysplastic kidney: about 18 cases].

Authors:  Hekmat Chaara; Hind Adadi; Imane Attar; Sofia Jayi; Fatima-Zahra Fdili Alaoui; Moulay Abdelilah Melhouf
Journal:  Pan Afr Med J       Date:  2019-07-31
  3 in total

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