Abstracto
Congenital glucose galactose malabsorption with hypercalcemia complicated with nephrogenic diabetes insipidus: Case report.
Yasmeen Al-Thawwad, Abdulmoein Eid Al-Agha
Glucose Galactose Malabsorption (GGM) is a rare inherited disorder complicated with hypercalcemia. The mechanism of hypercalcemia remains unclear. Nephrocalcinosis and reversable nephrogenic diabetes insipidus occurred as a complication of hypercalcemia. We report the case of female neonate with GGM and hypercalcemia complicated with NDI and nephrocalcinosis.
Descargo de responsabilidad: este resumen se tradujo utilizando herramientas de inteligencia artificial y aún no ha sido revisado ni verificado.