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Complete androgen insensitivity syndrome with accelerated onset of puberty due to a Sertoli cell tumor
Complete androgen insensitivity syndrome (CAIS) is caused by mutations in the androgen receptor gene. Patients with this syndrome have a 46,XY karyotype, male gonads, and normal female external genitalia. While the pre-pubertal risk of developing gonadal tumors is low in these patients, it increases...
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| Gepubliceerd in: | Clin Pediatr Endocrinol |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The Japanese Society for Pediatric Endocrinology
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8022032/ https://ncbi.nlm.nih.gov/pubmed/33867670 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.30.99 |
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