A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis
Abstract
Accumulating evidences suggest RET gene’s involvement in development of the kidney in mice and humans. Although it is well known that RET mutation causes multiple endocrine neoplasia type 2A (MEN2A), thus far only 3 individuals have been reported to have MEN2A and renal agenesis/dysgenesis. We report a MEN2A family with RET mutation in which two asymptomatic carriers presented with unilateral renal agenesis. A 48-year-old woman underwent total...
Paper Details
Title
A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis
Published Date
Jan 1, 2014
Journal
Volume
61
Issue
1
Pages
19 - 23
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