Article
Wilms' tumor and novel TRIM37 mutations in an Australian patient with mulibrey nanism.
Clinical genetics - 1 Dec 2006
Hämäläinen R H, Mowat D, Gabbett M T, O'brien T A, Kallijärvi J, Lehesjoki A-E
Abstract excerpt
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...
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