Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism

Hämäläinen, R. H., Mowat, D., Gabbett, M. T., O'Brien, T. A., Kallijärvi, J. and Lehesjoki, A. E. (2006) Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism. Clinical Genetics, 70 6: 473-479.


Author Hämäläinen, R. H.
Mowat, D.
Gabbett, M. T.
O'Brien, T. A.
Kallijärvi, J.
Lehesjoki, A. E.
Title Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism
Journal name Clinical Genetics   Check publisher's open access policy
ISSN 0009-9163
1399-0004
Publication date 2006-09-08
Sub-type Article (original research)
DOI 10.1111/j.1399-0004.2006.00700.x
Volume 70
Issue 6
Start page 473
End page 479
Total pages 7
Place of publication Oxford, United Kingdom
Publisher Wiley-Blackwell
Language eng
Subject 1103 Clinical Sciences
Formatted abstract Mulibrey nanism is a rare autosomal recessive growth disorder with prenatal onset, including occasional progressive cardiopathy, characteristic facial features, failure of sexual maturation, insulin resistance with type 2 diabetes, and an increased risk for Wilms' tumor. Mulibrey nanism is prevalent in the Finnish population and appears extremely rare elsewhere. However, cases outside of Finland may be underdiagnosed or misdiagnosed as having the 3-M or Silver–Russell syndrome, two important differential diagnostic disorders. Here, we report the first Australian patient with mulibrey nanism, in whom the occurrence of Wilms' tumor suggested the correct diagnosis. This was confirmed by the identification of two novel mutations in tripartite motif protein 37 (TRIM37) encoding a RING finger ubiquitin E3 ligase. Both mutations, the p.Cys109Ser B-box missense mutation and the p.Glu271_Ser287del in-frame deletion in the tumor necrosis factor receptor associated factor (TRAF) domain alter the subcellular localization of TRIM37. As both the B-box and the TRAF domains are predicted to be important for mediating the protein–protein interactions, these mutations may help the understanding of the cellular interactions of TRIM37. Our findings imply the importance of early molecular diagnostics in cases of suspected mulibrey nanism and of identifying novel mutations with potential relevance for unraveling the underlying molecular pathology. Ultrasound surveillance for Wilms' tumor is recommended for children with mulibrey nanism.
Keyword Growth disorder
Mulibrey
Nanism
Mutation
TRIM37
Wilms' tumor
Q-Index Code C1
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: Excellence in Research Australia (ERA) - Collection
School of Medicine Publications
 
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