Myelin Disorders Clinic, Pediatric Neurology Division, Children's Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
Faculty of Medicine, Students' Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Orphanet J Rare Dis. 2019 Jul 26;14(1):184. doi: 10.1186/s13023-019-1155-9.
Ribonucleases (RNases) are crucial for degradation of ribosomal RNA (rRNA). RNASET2 as a subtype of RNASEs is a 256 amino acid protein, encoded by RNASET2 gene located on chromosome six. Defective RNASET2 leads to RNASET2-deficient leukoencephalopathy, a rare autosomal recessive neurogenetic disorder with psychomotor delay as its main clinical symptom. The clinical findings can be similar to congenital cytomegalovirus (CMV) infection and Aicardi-Goutieres syndrome (AGS).
Herein, we presented a patient with motor delay, neurological regression, infrequent seizures and microcephaly at 5 months of age. Brain imaging showed white matter involvement, calcification and anterior temporal cysts. Basic metabolic tests, serum and urine CMV polymerase chain reaction (PCR) were requested. According to clinical and imaging findings, screening of RNASET2 and RMND1 genes were performed. The clinical data and magnetic resonance imaging (MRI) findings of previous reported individuals with RNASET2-deficient leukodystrophy were also reviewed and compared to the findings of our patient.
Brain MRI findings were suggestive of RNASET2-deficient leukoencephalopathy, AGS and CMV infection. Basic metabolic tests were normal and CMV PCR was negative. Molecular study revealed a novel homozygous variant of c.233C > A; p.Ser78Ter in exon 4 of RNASET2 gene compatible with the diagnosis of RNASET2-deficient leukoencephalopathy.
RNASET2-deficiency is a possible diagnosis in an infant presented with a static leukoencephalopathy and white matter involvement without megalencephaly. Due to overlapping clinical and radiologic features of RNASET2-deficient leukoencephalopathy, AGS and congenital CMV infections, molecular study as an important and helpful diagnostic tool should be considered to avoid misdiagnosis.
核糖核酸酶(RNases)对于核糖体 RNA(rRNA)的降解至关重要。RNASET2 作为 RNASEs 的一个亚型,是一种由位于染色体 6 上的 RNASET2 基因编码的 256 个氨基酸的蛋白质。RNASET2 缺陷导致 RNASET2 缺陷性脑白质病,这是一种罕见的常染色体隐性神经遗传疾病,以精神运动发育迟缓为主要临床症状。其临床表现可能与先天性巨细胞病毒(CMV)感染和 Aicardi-Goutières 综合征(AGS)相似。
本研究报道了一例 5 月龄时出现运动发育迟缓、神经退行性变、癫痫发作不频繁和小头畸形的患儿。脑部影像学显示白质受累、钙化和前颞部囊肿。我们要求进行基本代谢测试、血清和尿液 CMV 聚合酶链反应(PCR)。根据临床和影像学表现,对 RNASET2 和 RMND1 基因进行了筛查。还回顾了以前报道的 RNASET2 缺陷性脑白质营养不良患者的临床数据和磁共振成像(MRI)结果,并与我们患者的发现进行了比较。
脑部 MRI 结果提示 RNASET2 缺陷性脑白质病、AGS 和 CMV 感染。基本代谢测试正常,CMV-PCR 阴性。分子研究显示 RNASET2 基因外显子 4 中 c.233C > A; p.Ser78Ter 的新型纯合变异,符合 RNASET2 缺陷性脑白质病的诊断。
对于表现为静止性脑白质病和白质受累而无脑肿大的婴儿,RNASET2 缺陷可能是一种诊断。由于 RNASET2 缺陷性脑白质病、AGS 和先天性 CMV 感染的临床和影像学特征重叠,作为重要且有帮助的诊断工具的分子研究应予以考虑,以避免误诊。