Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension

• Glavni autori: Ossama K. Abou Hassan (Autor), Wiam Haidar (Autor), Mariam Arabi (Autor), Hadi Skouri (Autor), Fadi Bitar (Autor), Georges Nemer (Autor), Imad Bou Akl (Autor)
• Format: Knjiga
• Izdano: BMC, 2019-11-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

Abstract Background Pulmonary hypertension (PH) remains one of the rarest and deadliest diseases. Pulmonary Capillary Hemangiomatosis (PCH) is one of the sub-classes of PH. It was identified using histological and molecular tools and is characterized by the proliferation of capillaries into the alve...