Sekar Raja, Rajakumar Ilakyaa, Mathew Gerry G, Lamech Tanuj, Jayaprakash Varadharajan
Nephrology, SRM Medical College Hospital and Research Centre, Chengalpattu, IND.
Cureus. 2024 Jul 7;16(7):e64041. doi: 10.7759/cureus.64041. eCollection 2024 Jul.
A 25-year-old African male patient presented with a history of frothy urination for one month. He had a significant family history of early onset chronic kidney disease (CKD) in his older brother. On evaluation, he was found to have deranged renal function and nephrotic-range proteinuria of 6152 mg/day. Urine examination revealed proteinuria and glycosuria. Viral serology and autoimmune screening results were negative. Ultrasonography revealed contracted kidneys that were not amenable to biopsy. Genetic analysis revealed a Fanconi anemia-associated nuclease 1 (FAN 1) mutation in exon 4 (c.1399G>A) and exon 12 (c.2786A>C). The patient was managed conservatively with a maximum dose of angiotensin receptor blockers with a reduction in proteinuria on follow-up. This case report highlights the rare manifestation of FAN 1 mutation and its variable effects on the kidney.
一名25岁的非洲男性患者,有1个月的泡沫尿病史。他的哥哥有早发性慢性肾脏病(CKD)的显著家族史。经评估,发现他的肾功能紊乱,肾病范围蛋白尿为6152毫克/天。尿液检查显示蛋白尿和糖尿。病毒血清学和自身免疫筛查结果均为阴性。超声检查显示肾脏缩小,不适合进行活检。基因分析显示,外显子4(c.1399G>A)和外显子12(c.2786A>C)存在范可尼贫血相关核酸酶1(FAN 1)突变。该患者接受了最大剂量的血管紧张素受体阻滞剂保守治疗,随访时蛋白尿减少。本病例报告强调了FAN 1突变的罕见表现及其对肾脏的不同影响。