tailieunhanh - Fanconi syndrome and severe polyuria: An uncommon clinicobiological presentation of a Gitelman syndrome

Gitelman syndrome is an autosomal recessive tubulopathy characterized by hypokalemia, hypomagnesemia, metabolic alkalosis and hypocalciuria. The majority of patients do not present with symptoms until late childhood or adulthood, and the symptoms are generally mild. | Fanconi syndrome and severe polyuria: An uncommon clinicobiological presentation of a Gitelman syndrome

TỪ KHÓA LIÊN QUAN