Long W S, Seashore M R, Siegel N J, Bia M J
Yale University School of Medicine, New Haven, Connecticut.
Yale J Biol Med. 1990 Jan-Feb;63(1):15-28.
Fanconi syndrome is a complex of renal tubular dysfunctions defined by glycosuria without diabetes, aminoaciduria, phosphaturia, and renal tubular acidosis. It is often associated with hypokalemia, hypophosphatemia, and rickets or osteomalacia. Although it is usually found in the setting of other well-established non-renal diseases, Fanconi syndrome may present without identifiable etiology or association. Very infrequently a patient with idiopathic Fanconi syndrome will progress to chronic renal failure. This case report details the course of such a patient over the 20 years since his diagnosis and discusses the syndrome's genetic background, clinical features, putative pathophysiology, and therapeutic options, including transplantation.
范科尼综合征是一组肾小管功能障碍,其特征为非糖尿病性糖尿、氨基酸尿、磷酸盐尿和肾小管酸中毒。它常伴有低钾血症、低磷血症以及佝偻病或骨软化症。尽管范科尼综合征通常在其他已明确的非肾脏疾病背景下出现,但也可能无明确病因或关联。特发性范科尼综合征患者进展为慢性肾衰竭的情况非常罕见。本病例报告详细描述了一名患者自确诊以来20年的病程,并讨论了该综合征的遗传背景、临床特征、假定的病理生理学以及治疗选择,包括移植治疗。