Literature DB >> 3130862

Renal multicystic dysplasia: an occasional manifestation of the hereditary renal adysplasia syndrome.

E C Squiers1, R S Morden, J Bernstein.   

Abstract

Renal multicystic dysplasia is commonly regarded as a sporadic anomaly, although several studies of renal agenesis have shown the occasional occurrence of multicystic dysplasia in relatives of propositi with bilateral agenesis. We report the occurrence of unilateral multicystic dysplasia in an infant whose mother and maternal aunt had unilateral renal agenesis. The aunt's daughter, a first cousin of the proposita, had unilateral megaureter and hydronephrosis secondary to obstruction at the ureteropelvic junction. These observations suggest that nonsyndromal multicystic renal dysplasia can occur as part of the spectrum of hereditary renal adysplasia, with what appears to be autosomal dominant inheritance, and that the primary abnormality may reside in the ureter, with secondary renal maldevelopment.

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Year:  1987        PMID: 3130862     DOI: 10.1002/ajmg.1320280532

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  7 in total

1.  Early risk factors for neonatal mortality in CAKUT: analysis of 524 affected newborns.

Authors:  Batielhe F Melo; Marcos B Aguiar; Maria Candida F Bouzada; Regina L Aguiar; Alamanda K Pereira; Gabriela M Paixão; Mariana C Linhares; Flavia C Valerio; Ana Cristina Simões E Silva; Eduardo A Oliveira
Journal:  Pediatr Nephrol       Date:  2012-03-09       Impact factor: 3.714

2.  Is unilateral multicystic renal dysplasia sometimes heritable, and what is the risk of recurrence?

Authors:  J Bernstein
Journal:  Pediatr Nephrol       Date:  1990-11       Impact factor: 3.714

3.  Renal dysplasia: an autopsy study of associated congenital malformations.

Authors:  Z N Singh; A K Dinda
Journal:  Indian J Pediatr       Date:  1998 Mar-Apr       Impact factor: 1.967

4.  Implication of genetic variations in congenital obstructive nephropathy.

Authors:  Hyewon Hahn; So-Eun Ku; Kun-Suk Kim; Young-Seo Park; Chong-Hyun Yoon; Hae-Il Cheong
Journal:  Pediatr Nephrol       Date:  2005-08-25       Impact factor: 3.714

5.  A familial case of multicystic dysplastic kidney.

Authors:  Takashi Sekine; Yoshiyuki Namai; Atsuhiro Yanagisawa; Hiroshi Shirahama; Yukie Tashiro; Masahito Terahara; Michio Nagata; Yutaka Harita; Utako Fukuoka; Jun Inatomi; Takashi Igarashi
Journal:  Pediatr Nephrol       Date:  2005-06-23       Impact factor: 3.714

6.  Expression profiles of congenital renal dysplasia reveal new insights into renal development and disease.

Authors:  Sanjay Jain; Adrian A Suarez; John McGuire; Helen Liapis
Journal:  Pediatr Nephrol       Date:  2007-04-21       Impact factor: 3.714

7.  High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.

Authors:  Burcu Bulum; Z Birsin Ozçakar; Evren Ustüner; Ebru Düşünceli; Aslı Kavaz; Duygu Duman; Katherina Walz; Suat Fitoz; Mustafa Tekin; Fatoş Yalçınkaya
Journal:  Pediatr Nephrol       Date:  2013-06-28       Impact factor: 3.714

  7 in total

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