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Peutz-Jeghers syndrome a review of gynecological implications and the management of these patients through the presentation of a case report
Background: Peutz-Jeghers Syndrome (PJS) is a rare autosomal dominant genetic condition caused by mutations in STK11 (Serine/threonine kinase 11) gene (OMIM 602216 Serine/Threonine Protein Kinase 11) located in the short arm of chromosome 19 (19p.13.3). Case: We report the case of a 4 and ½ year-old...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
IMR Press
2022-04-01
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| Σειρά: | Clinical and Experimental Obstetrics & Gynecology |
| Θέματα: | |
| Διαθέσιμο Online: | https://www.imrpress.com/journal/CEOG/49/4/10.31083/j.ceog4904085 |
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