Breast ultrasound in the management of gynecomastia in Peutz–Jeghers syndrome in monozygotic twins: two case reports

INTRODUCTION: Peutz–Jeghers syndrome is an autosomal dominant disease with incomplete penetrance and variable expression caused by germline mutation of serine threonine kinase 11/liver kinase B1; it is characterized by hamartomatous polyps in the gastrointestinal tract, mucocutaneous melanin pigment...

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Detalles Bibliográficos
Autores principales: Di Grezia, Graziella, Romano, Tiziana, De Francesco, Francesco, Somma, Francesco, Rea, Gaetano, Grassi, Roberto, Gatta, Gianluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301923/
https://www.ncbi.nlm.nih.gov/pubmed/25519740
http://dx.doi.org/10.1186/1752-1947-8-440

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301923/
https://www.ncbi.nlm.nih.gov/pubmed/25519740
http://dx.doi.org/10.1186/1752-1947-8-440

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