Mammalian disorder of sexual development (Homo sapiens)
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Description
Multiple genes in the genital ridge are of importance for the formation of the bipotential ridge. Several of these genes are WT1, EMX2, PBX1, and CBX2. After 7 weeks there is a differentiation between XY and XX gonads.
In the XX gonad, the absence of the gene SRY will result in the under expression of the SOX9 gene. This will have as a consequence that the SOX9 gene will not reach its threshold. Along with the expression of RSPO1 and WNT4, β-catenin is signalled and will lead to further inhibition of SOX9 and stimulation of FST and FOXL2. Both RSPO1 and WNT, as well as the combination of FST and FOXL2 are stimulated by NR5A1. This process will lead to the formation of the ovary due to the suppression of the formation of the testis, by inhibition of the genes. Due to the absence of androgens the female reproductive system can develop.
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Bibliography
- Bashamboo A, McElreavey K; ''Mechanism of Sex Determination in Humans: Insights from Disorders of Sex Development.''; Sex Dev, 2016 PubMed Europe PMC Scholia
- Ostrer H; ''Disorders of sex development (DSDs): an update.''; J Clin Endocrinol Metab, 2014 PubMed Europe PMC Scholia
- Kyriakou, A, Lucas-Herald, A, McGowan, R, Tobias, E, Ahmed, F; ''Disorders of sex development: advances in genetic diagnosis and challenges in management ''; Dovepress, 10.2147/AGG.S53226, 2015 DOI Scholia
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