Jayasinghe K S, Mendis B L, Mohideen R, Ekanayake R, Sheriff M H, Dharmadasa K
Postgrad Med J. 1984 Apr;60(702):303-4. doi: 10.1136/pgmj.60.702.303.
Medullary sponge kidney associated with a defect in urine acidification is rare and usually of no clinical significance. We report a case presenting as hypokalaemic paralysis due to associated congenital distal renal tubular acidosis.
伴有尿酸化功能缺陷的髓质海绵肾较为罕见,通常无临床意义。我们报告一例因合并先天性远端肾小管酸中毒而表现为低钾性麻痹的病例。