Knapke Antje, Bourdat Michel Guylhène, Marey Isabelle, Le Tanno Pauline
Pediatrics, Grenoble University Hospital, Voiron, France.
Pediatrics, Grenoble University Hospital, Grenoble, France.
Front Pediatr. 2022 Feb 23;9:822114. doi: 10.3389/fped.2021.822114. eCollection 2021.
Cystinuria is a recessively inherited genetic disease causing recurrent kidney stones with risk of kidney failure. The discovery of hyperechoic colonic content on an antenatal ultrasound is considered to be a pathognomic sign of cystinuria. Herein, we present a clinical case with antenatal diagnosis of cystinuria in an ultrasound finding, which eventually revealed a multisystem disease, characterized by the association of renal Fanconi syndrome, hyperinsulinemic hypoglycemia, and hepatic dysfunction. Genetic investigations evidenced the recurrent heterozygous missense (p.Arg76Trp) variant. Our case report shows that antenatal hyperechoic colonic content can hide a complex proximal renal tubulopathy, and questions the genetic counseling provided to families in the antenatal period.
胱氨酸尿症是一种隐性遗传疾病,可导致复发性肾结石并有肾衰竭风险。产前超声检查发现结肠内容物高回声被认为是胱氨酸尿症的特征性体征。在此,我们报告一例产前超声诊断为胱氨酸尿症的临床病例,最终发现这是一种多系统疾病,其特征为肾范科尼综合征、高胰岛素血症性低血糖和肝功能障碍并存。基因检测证实存在复发性杂合错义(p.Arg76Trp)变异。我们的病例报告表明,产前结肠内容物高回声可能掩盖复杂的近端肾小管病,并对产前向家庭提供的遗传咨询提出质疑。