Nationwide Turkish Cohort Study of Hypophosphatemic Rickets

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...

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Publicado en:J Clin Res Pediatr Endocrinol
Autores principales: Şıklar, Zeynep, Turan, Serap, Bereket, Abdullah, Baş, Firdevs, Güran, Tülay, Akberzade, Azad, Abacı, Ayhan, Demir, Korcan, Böber, Ece, Özbek, Mehmet Nuri, Kara, Cengiz, Poyrazoğlu, Şükran, Aydın, Murat, Kardelen, Aslı, Tarım, Ömer, Eren, Erdal, Hatipoğlu, Nihal, Büyükinan, Muammer, Akyürek, Nesibe, Çetinkaya, Semra, Bayramoğlu, Elvan, Selver Eklioğlu, Beray, Uçaktürk, Ahmet, Abalı, Saygın, Gökşen, Damla, Kor, Yılmaz, Ünal, Edip, Esen, İhsan, Yıldırım, Ruken, Akın, Onur, Çayır, Atilla, Dilek, Emine, Kırel, Birgül, Anık, Ahmet, Çatlı, Gönül, Berberoğlu, Merih
Formato: Artigo
Lenguaje:Inglês
Publicado: Galenos Publishing 2020
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Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7291408/
https://ncbi.nlm.nih.gov/pubmed/31514490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.galenos.2019.2019.0098
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