Literature DB >> 3130865

Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases.

A V Moorthy1, R W Chesney, M Lubinsky.   

Abstract

The development of chronic renal failure because of parenchymatous renal disease in patients in 46,XY gonadal dysgenesis was noted initially by Drash et al [J Pediatr 76:585-593, 1970]. However, we think that some of the cases reported as examples of the Drash syndrome are a different disorder. In this paper, we review six previously reported patients with streak gonads, pseudohermaphroditism, and renal failure. In several of these patients the diagnosis was established only after a successful kidney transplantation during evaluation for primary amenorrhea. Gonadoblastoma arising from the streak gonad was noted in five of the six patients. "Frasier" syndrome would be a suitable term to denote this association after Frasier et al, who described two patients in 1964. We recommend evaluation of the gonads in prepubertal girls with end-stage renal disease at risk for this syndrome.

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Year:  1987        PMID: 3130865     DOI: 10.1002/ajmg.1320280535

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


  18 in total

1.  Twenty-eight-year-old female with primary amenorrhea and chronic renal failure: a case of Frasier syndrome?

Authors:  Raphael Onyemekeihia; Efosa Oviasu
Journal:  J Natl Med Assoc       Date:  2004-02       Impact factor: 1.798

2.  WT1 gene mutations in three girls with nephrotic syndrome.

Authors:  Khalid Ismaili; Véronique Verdure; Katherina Vandenhoute; Françoise Janssen; Michelle Hall
Journal:  Eur J Pediatr       Date:  2007-06-01       Impact factor: 3.183

3.  What investigations are appropriate in a teenage girl with chronic renal failure who has primary amenorrhea?

Authors:  R W Chesney; S Burstein
Journal:  Pediatr Nephrol       Date:  1991-09       Impact factor: 3.714

Review 4.  From ureteric bud to the first glomeruli: genes, mediators, kidney alterations.

Authors:  Vassilios Fanos; Cristina Loddo; Melania Puddu; Clara Gerosa; Daniela Fanni; Giovanni Ottonello; Gavino Faa
Journal:  Int Urol Nephrol       Date:  2014-09-09       Impact factor: 2.370

5.  WT1 intron 9 splice acceptor site mutation in a 46,XY male with focal segmental glomerulosclerosis.

Authors:  Katsuyoshi Kanemoto; Kenji Ishikura; Daisuke Ariyasu; Yuko Hamasaki; Hiroshi Hataya; Yukihiro Hasegawa; Masahiro Ikeda
Journal:  Pediatr Nephrol       Date:  2006-10-24       Impact factor: 3.714

Review 6.  The Denys-Drash syndrome.

Authors:  R F Mueller
Journal:  J Med Genet       Date:  1994-06       Impact factor: 6.318

7.  Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation.

Authors:  Pietro Dattolo; Marco Allinovi; Paraskevas Iatropoulos; Stefano Michelassi
Journal:  BMJ Case Rep       Date:  2013-05-27

Review 8.  Nephrotic syndrome in the 1st year of life.

Authors:  R Habib
Journal:  Pediatr Nephrol       Date:  1993-08       Impact factor: 3.714

9.  Frasier syndrome, a potential cause of end-stage renal failure in childhood.

Authors:  Manon Bache; Céline Dheu; Bérénice Doray; Hélène Fothergill; Sylvie Soskin; Françoise Paris; Charles Sultan; Michel Fischbach
Journal:  Pediatr Nephrol       Date:  2010-03       Impact factor: 3.714

10.  Genetic forms of nephrotic syndrome: a single-center experience in Brussels.

Authors:  Khalid Ismaili; Audrey Pawtowski; Olivia Boyer; Karl Martin Wissing; Françoise Janssen; Michelle Hall
Journal:  Pediatr Nephrol       Date:  2008-08-16       Impact factor: 3.714

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