Mansukhani Sasha, Ho Mai Lan, Gavrilova Ralitza H, Mohney Brian G, Quiram Polly A, Brodsky Michael C
Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota.
Department of Radiology, Mayo Clinic, Rochester, Minnesota.
J AAPOS. 2017 Oct;21(5):420-422. doi: 10.1016/j.jaapos.2017.04.015. Epub 2017 Aug 31.
An 8-month-old girl presented with vitreous hemorrhage, peripheral retinal arteriovenous anastomosis, and hypoplasia of the thumb. Magnetic resonance imaging of the brain showed multiple hyperintensities, cysts, and calcifications in the white matter. DNA testing showed a mutation in one allele of the CTC gene, supporting the diagnosis of cerebroretinal microangiopathy with calcifications and cysts (CRMCC), or Coats plus disease, despite which designation this condition can present without subretinal exudate. In infants with peripheral retinal vascular disease, neuroimaging can identify the characteristic abnormalities of CRMCC.
一名8个月大的女孩出现玻璃体出血、周边视网膜动静脉吻合以及拇指发育不全。脑部磁共振成像显示白质有多处高信号、囊肿和钙化。DNA检测显示CTC基因的一个等位基因发生突变,支持钙化和囊肿性脑视网膜微血管病(CRMCC)或科茨加综合征的诊断,尽管这种疾病可能在没有视网膜下渗出液的情况下出现。对于患有周边视网膜血管疾病的婴儿,神经影像学检查可识别CRMCC的特征性异常。