Barakat A J, Arianas P, Glick A D, Butler M G
Department of Pediatrics, Georgetown University Medical Center, Washington, D.C.
Child Nephrol Urol. 1990;10(2):109-11.
We report a 6-year-old white male with Laurence-Moon-Biedl syndrome and focal sclerosing glomerulonephritis (FSGN). To our knowledge, FSGN has not been reported previously in patients with this syndrome. We wish to alert the clinician to the wide variety of renal abnormalities that can be seen in patients with this rare, autosomal recessive disorder.
我们报告了一名患有劳伦斯-穆恩-比德尔综合征和局灶性硬化性肾小球肾炎(FSGN)的6岁白人男性。据我们所知,此前尚未有关于该综合征患者发生FSGN的报道。我们希望提醒临床医生注意,在这种罕见的常染色体隐性疾病患者中可能会出现各种各样的肾脏异常情况。