Disease Manifestations and Complications in Dutch X-Linked Hypophosphatemia Patients
X-linked hypophosphatemia (XLH) is the most common monogenetic cause of chronic hypophosphatemia, characterized by rickets and osteomalacia. Disease manifestations and treatment of XLH patients in the Netherlands are currently unknown. Characteristics of XLH patients participating in the Dutch observational registry for genetic hypophosphatemia and acquired renal phosphate wasting were analyzed. Eighty XLH patients, including 29 children, were included. Genetic testing, performed in 78.8% of patients, showed a PHEX mutation in 96.8%. Median (range) Z-score for height was − 2.5 (− 5.5; 1.0) in... Mehr ...
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| Dokumenttyp: | Artikel |
| Erscheinungsdatum: | 2024 |
| Reihe/Periodikum: | Bosman , A , Appelman-Dijkstra , N M , Boot , A M , de Borst , M H , van de Ven , A C , de Jongh , R T , Bökenkamp , A , van den Bergh , J P , van der Eerden , B C J & Zillikens , M C 2024 , ' Disease Manifestations and Complications in Dutch X-Linked Hypophosphatemia Patients ' , Calcified tissue international , vol. 114 , no. 3 , pp. 255-266 . https://doi.org/10.1007/s00223-023-01172-2 |
| Schlagwörter: | FGF23 / Hypophosphatemia / Phosphate / X-linked hypophosphatemia / XLH |
| Sprache: | Englisch |
| Permalink: | https://search.fid-benelux.de/Record/base-29029195 |
| Datenquelle: | BASE; Originalkatalog |
| Powered By: | BASE |
| Link(s) : | https://hdl.handle.net/11370/f30ea9da-659d-40b6-82c8-cbd889f4bfa7 |
