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HERO ID
7439238
Reference Type
Journal Article
Title
46,XY DSD
Author(s)
O’Connell, MA; Bouty, A; Grover, SR; ,
Year
2020
Publisher
Springer Singapore
Location
Singapore
Book Title
Disorders|Differences of Sex Development
Page Numbers
77-102
DOI
10.1007/978-981-13-7864-5_7
URL
http://link.springer.com/10.1007/978-981-13-7864-5_7
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Abstract
DSD, with 46,XY chromosomal complement, comprise a heterogeneous group of conditions, where either the hormones associated with virilisation (androgens) are not produced, or the target organs are unable to respond in a typical manner. Important causes to consider in these individuals are gonadal dysgenesis, variations in androgen synthesis and androgen insensitivity syndrome (AIS)—partial or complete. However, the precise nature of many 46,XY DSD cannot be diagnosed at a molecular level. Improved identification of the underlying molecular variations will hopefully allow for improved understanding of outcomes and management options.
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