renal hypouricosuria is often caused by a genetic mutation in the urat1 transporter.
肾性低尿酸血症通常是由urat1转运蛋白的基因突变引起的。
patients with hypouricosuria typically exhibit low serum uric acid levels in blood tests.
低尿酸血症患者在血液检查中通常显示血清尿酸水平偏低。
exercise-induced acute kidney injury is a known complication of hypouricosuria.
运动诱发的急性肾损伤是低尿酸血症的一种已知并发症。
doctors diagnose hypouricosuria by measuring the fractional excretion of uric acid.
医生通过测量尿酸排泄分数来诊断低尿酸血症。
idiopathic hypouricosuria can predispose individuals to forming uric acid stones.
特发性低尿酸血症可能使个体易患尿酸结石。
medication usage is generally unnecessary for asymptomatic cases of hypouricosuria.
对于无症状的低尿酸血症病例，通常不需要使用药物治疗。
differential diagnosis of hypouricosuria includes fanconi syndrome and wilson disease.
低尿酸血症的鉴别诊断包括范可尼综合征和威尔逊氏病。
genetic testing can confirm hereditary renal hypouricosuria in young patients.
基因检测可以确诊年轻患者的遗传性肾性低尿酸血症。
severe hypouricosuria may lead to exercise-induced rhabdomyolysis in rare instances.
在极少数情况下，严重的低尿酸血症可能导致运动诱发的横纹肌溶解。
management of hypouricosuria focuses primarily on preventing dehydration during physical activity.
低尿酸血症的管理主要集中在防止体力活动期间的脱水。
the pathophysiology of hypouricosuria involves impaired reabsorption in the proximal tubule.
低尿酸血症的病理生理学涉及近端小管重吸收受损。
screening for hypouricosuria is recommended for family members of affected patients.
建议对患者家属进行低尿酸血症筛查。
renal hypouricosuria is often caused by a genetic mutation in the urat1 transporter.
肾性低尿酸血症通常是由urat1转运蛋白的基因突变引起的。
patients with hypouricosuria typically exhibit low serum uric acid levels in blood tests.
低尿酸血症患者在血液检查中通常显示血清尿酸水平偏低。
exercise-induced acute kidney injury is a known complication of hypouricosuria.
运动诱发的急性肾损伤是低尿酸血症的一种已知并发症。
doctors diagnose hypouricosuria by measuring the fractional excretion of uric acid.
医生通过测量尿酸排泄分数来诊断低尿酸血症。
idiopathic hypouricosuria can predispose individuals to forming uric acid stones.
特发性低尿酸血症可能使个体易患尿酸结石。
medication usage is generally unnecessary for asymptomatic cases of hypouricosuria.
对于无症状的低尿酸血症病例，通常不需要使用药物治疗。
differential diagnosis of hypouricosuria includes fanconi syndrome and wilson disease.
低尿酸血症的鉴别诊断包括范可尼综合征和威尔逊氏病。
genetic testing can confirm hereditary renal hypouricosuria in young patients.
基因检测可以确诊年轻患者的遗传性肾性低尿酸血症。
severe hypouricosuria may lead to exercise-induced rhabdomyolysis in rare instances.
在极少数情况下，严重的低尿酸血症可能导致运动诱发的横纹肌溶解。
management of hypouricosuria focuses primarily on preventing dehydration during physical activity.
低尿酸血症的管理主要集中在防止体力活动期间的脱水。
the pathophysiology of hypouricosuria involves impaired reabsorption in the proximal tubule.
低尿酸血症的病理生理学涉及近端小管重吸收受损。
screening for hypouricosuria is recommended for family members of affected patients.
建议对患者家属进行低尿酸血症筛查。
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