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European Journal of Pediatrics

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01-12-2013 | Correspondence

Different clinical presentations of WT1 gene mutations

Authors: Mustafa Aydin, Nilay Hakan, Aysegul Zenciroglu, Ozlem Aydog, Nurullah Okumus

Published in: European Journal of Pediatrics | Issue 12/2013

Excerpt

Dear Editor, …

Hakan N, Aydin M, Erdogan O, Cavusoglu YH, Aycan Z, Ozaltin F, Zenciroglu A, Apaydin S, Gunes R, Sahin G, Cinar G, Okumus N, Hakan N, Aydin M, Erdogan O et al (2012) A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome. Genet Couns 23:255–261PubMed

Kreidberg JA (2010) WT1 and kidney progenitor cells. Organogenesis 6:61–70PubMedCrossRef

Mueller RF (1994) The Denys-Drash syndrome. J Med Genet 31:471–477PubMedCrossRef

Yang Y, Feng D, Huang J, Nie X, Yu Z, Yang Y, Feng D, Huang J et al (2013) A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male. Eur J Pediatr 172:127–129PubMedCrossRef

Title: Different clinical presentations of WT1 gene mutations
Authors: Mustafa Aydin
Nilay Hakan
Aysegul Zenciroglu
Ozlem Aydog
Nurullah Okumus
Publication date: 01-12-2013
Publisher: Springer Berlin Heidelberg
Published in: European Journal of Pediatrics / Issue 12/2013
Print ISSN: 0340-6199
Electronic ISSN: 1432-1076
DOI: https://doi.org/10.1007/s00431-013-2085-5

At a glance: The STEP trials

Springer Medicine

Different clinical presentations of WT1 gene mutations

Excerpt

At a glance: The STEP trials

Springer Medicine

Excerpt

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