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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.

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