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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Bibliografiska uppgifter
I publikationen:J Med Case Rep
Huvudupphovsmän: Di Grezia, Graziella, Romano, Tiziana, De Francesco, Francesco, Somma, Francesco, Rea, Gaetano, Grassi, Roberto, Gatta, Gianluca
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2014
Ämnen:
Case Report
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4301923/
https://ncbi.nlm.nih.gov/pubmed/25519740
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-1947-8-440
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