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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Main Authors: Katarzyna Plagens-Rotman (Author), Grażyna Jarząbek-Bielecka (Author), Piotr Merks (Author), Katarzyna Wróblewska-Seniuk (Author), Małgorzata Mizgier (Author), Ewa Jakubek (Author), Samuel Grześkiewicz (Author), Małgorzata Wójcik (Author), Witold Kędzia (Author)
Format: Book
Published: IMR Press, 2022-04-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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