Cowden syndrome- Clinico-radiological illustration of a rare case

• Autors principals: Prashant B Patil (Autor), V Sreenivasan (Autor), Sumit Goel (Autor), K Nagaraju (Autor), Shirin Vashishth (Autor), Swati Gupta (Autor), Kanika Garg (Autor)
• Format: Llibre
• Publicat: Wolters Kluwer Medknow Publications, 2013-01-01T00:00:00Z.
• Matèries: article
• Accés en línia: Connect to this object online.

Cowden syndrome (CS) or multiple hamartoma syndrome is an infrequent genodermatoses, which is inherited as an autosomal dominant trait resulting from the mutation in the Phosphatase and Tensin homolog gene on the arm 10q and is principally characterized by multiple hamartomas with an increased risk...