TY  - JOUR
AU  - Castellano-Martinez, Ana
AU  - Acuñas-Soto, Silvia
AU  - Roldan-Cano, Virginia
AU  - Rodriguez-Gonzalez, Moises
PY  - 2021
DO  - 10.4274/jcrpe.galenos.2021.2020.0287
UR  - http://hdl.handle.net/10668/21637
T2  - Journal of clinical research in pediatric endocrinology
AB  - X-linked hypophosphatemia (XLH) is a rare genetic disorder with X-linked dominant inheritance. Mutations in the PHEX gene increase fibroblast growth factor 23 (FGF23) concentrations, causing loss of phosphorus at the proximal tubule. Most pediatric...
LA  - en
KW  - FGF23
KW  - X-linked hypophosphataemia
KW  - arterial hypertension
KW  - cardiovascular risk
KW  - left ventricular hypertrophy
KW  - burosumab
KW  - Familial Hypophosphatemic Rickets
KW  - Fibroblast Growth Factors
KW  - Humans
KW  - Hypertrophy, Left Ventricular
KW  - Phosphorus
KW  - Quality of Life
TI  - Left Ventricular Hypertrophy in Patients with X-Linked Hypophosphataemia.
TY  - research article
VL  - 14
ER  -