Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

• Glavni autori: Zeynep Şıklar (Autor), Serap Turan (Autor), Abdullah Bereket (Autor), Firdevs Baş (Autor), Tülay Güran (Autor), Azad Akberzade (Autor), Ayhan Abacı (Autor), Korcan Demir (Autor), Ece Böber (Autor), Mehmet Nuri Özbek (Autor), Cengiz Kara (Autor), Şükran Poyrazoğlu (Autor), Murat Aydın (Autor), Aslı Kardelen (Autor), Ömer Tarım (Autor), Erdal Eren (Autor), Nihal Hatipoğlu (Autor), Muammer Büyükinan (Autor), Nesibe Akyürek (Autor), Semra Çetinkaya (Autor), Elvan Bayramoğlu (Autor), Beray Selver Eklioğlu (Autor), Ahmet Uçaktürk (Autor), Saygın Abalı (Autor), Damla Gökşen (Autor), Yılmaz Kor (Autor), Edip Ünal (Autor), İhsan Esen (Autor), Ruken Yıldırım (Autor), Onur Akın (Autor), Atilla Çayır (Autor), Emine Dilek (Autor), Birgül Kırel (Autor), Ahmet Anık (Autor), Gönül Çatlı (Autor), Merih Berberoğlu (Autor)
• Format: Knjiga
• Izdano: Galenos Yayincilik, 2020-06-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

Objective:Hypophosphatemic rickets (HR) is a rare renal phosphate-wasting disorder, which is usually X-linked and is commonly caused by PHEX mutations. The treatment and follow-up of HR is challenging due to imperfect treatment options.Methods:Here we present nationwide initial and follow-up data on...