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...

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Detaylı Bibliyografya
Asıl Yazarlar: Katarzyna Plagens-Rotman, Grażyna Jarząbek-Bielecka, Piotr Merks, Katarzyna Wróblewska-Seniuk, Małgorzata Mizgier, Ewa Jakubek, Samuel Grześkiewicz, Małgorzata Wójcik, Witold Kędzia
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: IMR Press 2022-04-01
Seri Bilgileri:Clinical and Experimental Obstetrics & Gynecology
Konular:
children
polyposis
peutz-jeghers syndrome
Online Erişim:https://www.imrpress.com/journal/CEOG/49/4/10.31083/j.ceog4904085
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