Department of Radiology and Molecular Imaging, Sultan Qaboos University Hospital, Muscat, Oman.
Child Health Department, Sultan Qaboos University Hospital, Muscat, Oman.
Neuroradiol J. 2023 Dec;36(6):740-745. doi: 10.1177/19714009231154677. Epub 2023 Feb 1.
Aicardi-Goutières syndrome (AGS) is an autosomal recessive disease that mimics congenital viral infection and mainly affects the brain, immune system, and skin. The dominant clinical symptom is the subacute onset of severe encephalopathy, which manifests as irritability, loss of ability, slowing of head growth, and poor nutrition. Arteriopathy in AGS is an uncommon manifestation usually associated with mutations in the SAMHD1 gene. We present a rare case of a 3-year-old male due to failure to thrive, global developmental delay, microcephaly, poor vision, upper and lower limbs spasticity, and gastroesophageal reflux disease (GERD), who harbored early stenotic lesions of the large and medium intracranial arteries with ischemic sequelae in the early postnatal life. Performed genetic testing confirmed homozygous gene mutation, SAMHD1 associated with AGS type 5. By reviewing the available literature, we were able to find only one patient whose arterial lesions were diagnosed after 6 months.
Aicardi-Goutières 综合征(AGS)是一种常染色体隐性疾病,模拟先天性病毒感染,主要影响大脑、免疫系统和皮肤。主要的临床症状是亚急性发作的严重脑病,表现为烦躁、丧失能力、头围生长缓慢和营养状况不佳。AGS 的血管病变是一种不常见的表现,通常与 SAMHD1 基因的突变有关。我们报告了一例罕见的 3 岁男性病例,因生长不良、全面发育迟缓、小头畸形、视力差、上下肢痉挛和胃食管反流病(GERD)就诊,该患儿在新生儿期后即存在大中颅内动脉早期狭窄病变和缺血后遗症。进行的基因检测证实存在与 AGS 类型 5 相关的纯合基因突变 SAMHD1。通过回顾现有文献,我们仅发现一例患者在 6 个月后被诊断为动脉病变。