Hypergonadotropic hypogonadism and renal failure due to WT1 mutation

Author:

Benz Kerstin,Plank Christian,Amann Kerstin,Mucha Bettina,Dörr Helmuth G.,Rascher Wolfgang,Dötsch Jörg

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference15 articles.

1. Oertel PJ, Lichtwald K, Hafner S, Rauh W, Schonberg D, Scharer K. Hypothalamo-pituitary-gonadal axis in children with chronic renal failure. Kidney Int Suppl1983; 15: 34–39

2. Schaefer F, Mehls O. Endocrine and growth disturbances. In: Barrat TM, Avner ED, Harmon WE, eds. Pediatric Nephrology, 4th edn. Lippincott Williams and Wilkins, Baltimore: 1999; 1197–1230

3. Sinnecker GH, Hiort O, Dibbelt L et al. Phenotypic classification of male pseudohermaphroditism due to steroid 5 alpha-reductase 2 deficiency. Am J Med Genet1996; 63: 223–230

4. Melo KF, Martin RM, Costa EM et al. An unusual phenotype of Frasier syndrome due to IVS9 + 4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis. J Clin Endocrinol Metab2002; 87: 2500–2505

5. Frasier SD, Bashore RA, Mosier HD. Gonadoblastoma associated with pure gonadal dysgenesis in monozygous twins. J Pediatr1964; 64: 740–745

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