Fetal brain small vessel disease 1 caused by a novel mutation in the COL4A1 gene.
Elizabeth C EnglandPatricia CornejoDerek E NeilsonRashmi P RaoLuis F GoncalvesPublished in: Pediatric radiology (2020)
A singleton fetus was referred to fetal magnetic resonance imaging (MRI) at 25 weeks due to mild ventriculomegaly and an abnormal fetal echocardiogram showing cardiomegaly, right ventricular hypertrophy and tricuspid insufficiency. Patchy areas of ischemic infarction, extensive subacute and chronic hemorrhage not respecting vascular territories, encephaloclastic cysts and closed lip schizencephaly were identified. Cataract was detected postnatally. The anomalies were caused by a pathogenic mutation (c.353 G>A; p.G118D) in the COL4A1 gene. The phenotype seen in this case, i.e. small vessel cerebral disease with or without ocular anomalies caused by COL4A1 mutations, is likely an underrecognized cause of perinatal stroke. The pattern of abnormalities reported herein should prompt strong consideration for diagnosis and molecular testing.
Keyphrases
- magnetic resonance imaging
- cerebral ischemia
- genome wide
- contrast enhanced
- copy number
- computed tomography
- gestational age
- atrial fibrillation
- genome wide identification
- mitral valve
- aortic valve
- transcatheter aortic valve replacement
- coronary artery disease
- dna methylation
- magnetic resonance
- single molecule
- multiple sclerosis
- physical activity
- gene expression
- left ventricular
- resting state
- optic nerve
- weight loss