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

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Abstract

The diagnosis of Frasier syndrome is based on the association of male pseudohermaphroditism (as a result of gonadal dysgenesis), with steroid-resistant nephrotic syndrome due to focal and segmental glomerular sclerosis (FSGS), which progresses to end-stage renal failure (ESRF) during adolescence or adulthood. Frasier syndrome results from mutations in the Wilms’ tumour suppressor gene WT1, which is responsible for alterations in male genital development and podocyte dysfunction. We describe the case of a 7-year-old girl who was referred to the paediatric emergency department with ESRF. Haemodialysis was started immediately because of severe hypertension and hyperkalaemia. In view of the fact that our patient had a past medical history of pseudohermaphroditism, we suspected that the acute presentation in ESRF may be related to a new diagnosis of Frasier syndrome. Our hypothesis was confirmed on examination of the medical records. There had been no medical follow-up for several years and, in particular, no renal imaging or functional assessment had ever been performed. This lack of surveillance explains why our patient presented with ESRF much earlier in this disease than expected and subsequently had to undergo kidney transplantation at a very young age.

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References

  1. Frasier SD, Bashore RA, Mosier HD (1964) Gonadoblastoma associated with pure gonadal dysgenesis in monozygotic twins. J Pediatr 64:740–745

    Article  CAS  PubMed  Google Scholar 

  2. Barbaux S, Niaudet P, Gubler MC, Grunfeld JP, Jaubert F, Kuttenn F, Fekete CN, Souleyreau Therville N, Thibaud E, Fellous M, McElreavey K (1997) Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat Genet 17:467–470

    Article  CAS  PubMed  Google Scholar 

  3. Gubler MC, Yang Y, Jeanpierre C, Barbaux S, Niaudet P (1999) WT1, renal development, and glomerulopathies. Adv Nephrol Necker Hosp 29:299–315

    CAS  PubMed  Google Scholar 

  4. Moorthy AV, Chesney RW, Lubinsky M (1987) Chronic renal failure and XY gonadal dysgenesis: “Frasier” syndrome, a commentary on reported cases. Am J Med Genet 3:297–302

    Article  CAS  Google Scholar 

  5. Demmer L, Primack W, Loik V, Brown R, Therville N, McElreavey K (1999) Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46, XX female. J Am Soc Nephrol 10:2215–2218

    CAS  PubMed  Google Scholar 

  6. Loirat C, Andre JL, Champigneulle J, Acquaviva C, Chantereau D, Bourquard R, Elion J, Denamur E (2003) WT1 splice site mutation in a 46, XX female with minimal-change nephrotic syndrome and Wilms’ tumour. Nephrol Dial Transplant 18:823–825

    Article  CAS  PubMed  Google Scholar 

  7. Barbosa AS, Hadjiathanasiou CG, Theodoridis C, Papathanasiou A, Tar A, Merksz M, Gyorvari B, Sultan C, Dumas R, Jaubert F, Niaudet P, Moreira-Filho CA, Cotinot C, Fellous M (1999) The same mutation affecting the splicing of WT1 gene is present in Frasier syndrome patients with or without Wilms’ tumor. Hum Mutat 13:146–153

    Article  CAS  PubMed  Google Scholar 

  8. Niaudet P, Gubler MC (2006) WT1 and glomerular diseases. Pediatr Nephrol 21:1653–1660

    Article  PubMed  Google Scholar 

  9. Kikuchi H, Takata A, Akasaka Y, Fukuzawa R, Yoneyama H, Kurosawa Y, Honda M, Kamiyama Y, Hata J (1998) Do intronic mutations affecting splicing of WT1 exon 9 cause Frasier syndrome? J Med Genet 35:45–48

    Article  CAS  PubMed  Google Scholar 

  10. Klamt B, Koziell A, Poulat F, Wieacker P, Scambler P, Berta P, Gessler M (1998) Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms. Hum Mol Genet 7:709–714

    Article  CAS  PubMed  Google Scholar 

  11. Bruening W, Bardeesy N, Silverman BL, Cohn RA, Machin GA, Aronson AJ, Housman D, Pelletier J (1992) Germline mutations in the Wilms’ tumor gene (WT1) affecting urogenital development. Nat Genet 1:144–148

    Article  CAS  PubMed  Google Scholar 

  12. Okuhara K, Tajima S, Nakae J, Sasaki S, Tochimaru H, Abe S, Fujieda K (1999) A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene. Endocr J 46:639–642

    Article  CAS  PubMed  Google Scholar 

  13. Bonte A, Schroder W, Denamur E, Querfeld U (2000) Absent pubertal development in a child with chronic renal failure: the case of Frasier syndrome. Nephrol Dial Transplant 15:1688–1690

    Article  CAS  PubMed  Google Scholar 

  14. Buzi F, Mella P, Pilotta A, Felappi B, Camerino G, Notarangelo LD (2001) Frasier syndrome with childhood-onset renal failure. Horm Res 55:77–80

    Article  CAS  PubMed  Google Scholar 

  15. Shimoyama H, Nakajima M, Naka H, Park YD, Hori K, Morikawa H, Yoshioka A (2002) A girl with bilateral ovarian tumours: Frasier syndrome. Eur J Pediatr 161:81–83

    Article  PubMed  Google Scholar 

  16. Joki-Erkkila MM, Karikoski R, Rantala I, Lenko HL, Visakorpi T, Heinonen PK (2002) Gonadoblastoma and dysgerminoma associated with XY gonadal dysgenesis in an adolescent with chronic renal failure: a case of Frasier syndrome. J Pediatr Adolesc Gynecol 15:145–149

    Article  PubMed  Google Scholar 

  17. Chak WL, To KF, Cheng YL, Tsui KM, Lo KL, Tong HM, Lai FM, Wong FK, Choi KS, Chau KF, Li CS (2002) Gonadal mosaicism of Frasier syndrome in 3 Chinese siblings with donor splice site mutation of Wilms’ tumour gene. Nephron 91:526–529

    Article  CAS  PubMed  Google Scholar 

  18. Wang NJ, Song HR, Schanen NC, Litman NL, Frasier SD (2005) Frasier syndrome comes full circle: genetic studies performed in an original patient. J Pediatr 146:843–844

    Article  PubMed  Google Scholar 

  19. Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE (1991) WT1 mutations contribute to abnormal genital system development and hereditary Wilms’ tumor. Nature 353:431–434

    Article  CAS  PubMed  Google Scholar 

  20. Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jaenisch R (1993) WT-1 is required for early kidney development. Cell 74:679–691

    Article  CAS  PubMed  Google Scholar 

  21. Auber F, Jeanpierre C, Denamur E, Jaubert F, Schleiermacher G, Patte C, Cabrol S, Leverger G, Nihoul-Fékété C, Sarnacki S (2009) Management of Wilms tumors in Drash and Frasier syndromes. Pediatr Blood Cancer 52:55–59

    Article  CAS  PubMed  Google Scholar 

  22. König A, Jakubiczka S, Wieacker P, Schlosser HW, Gessler M (1993) Further evidence that imbalance of WT1 isoforms may be involved in Denys-Drash syndrome. Hum Mol Genet 2:1967–1968

    Article  PubMed  Google Scholar 

  23. Gwin K, Cajaiba MM, Caminoa-Lizarralde A, Picazo ML, Nistal M, Reyes-Mugica M (2008) Expanding the clinical spectrum of Frasier syndrome. Pediatr Dev Pathol 11:122–127

    Article  PubMed  Google Scholar 

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Correspondence to Charles Sultan or Michel Fischbach.

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Bache, M., Dheu, C., Doray, B. et al. Frasier syndrome, a potential cause of end-stage renal failure in childhood. Pediatr Nephrol 25, 549–552 (2010). https://doi.org/10.1007/s00467-009-1343-2

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  • DOI: https://doi.org/10.1007/s00467-009-1343-2

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