Left Ventricular Hypertrophy in Patients with X-Linked Hypophosphataemia

• Päätekijät: Ana Castellano-Martinez (Tekijä), Silvia Acuñas-soto (Tekijä), Virginia Roldan-cano (Tekijä), Moises Rodriguez-Gonzalez (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Galenos Yayincilik, 2022-09-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

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 patients debut in the first two years with short st...