| Literature DB >> 29591721 |
Krishnan Nagarajan1, Elango Swamiappan1, Sathiaprabhu Anbazhagan1, Ashwin Dalal2, Subathra Adithan1, Timo Krings3.
Abstract
ACTA2 mutations are recently described genetically defined abnormalities of blood vessels in various organs of the body with specific abnormalities in cerebral vessels in the form of straightening of all cerebral arteries ("twig-like" pattern), stenosis/occlusions, proximal dilatation, and absent "moyamoya" type of collaterals. We describe a one-and-a half year-old girl child who presented with mild motor developmental delay and on neuroimaging showed septo-preoptic holoprosencephaly, diffuse radial polymicrogyria, and pontine hypoplasia along with magnetic resonance angiographic features suggestive of ACTA2 mutation type of cerebral vessels. However, genetic studies revealed no evidence of ACTA2 mutation, indicating that the "twig-like" pattern may not only be a pathognomonic feature of ACTA2 mutations.Entities:
Keywords: ACTA2-related cerebrovascular disease; embryonic cerebral vasculature; magnetic resonance angiography; polymicrogyria; pontine hypoplasia; septo-preoptic holoprosencephaly
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Year: 2018 PMID: 29591721 PMCID: PMC6050896 DOI: 10.1177/1591019918765239
Source DB: PubMed Journal: Interv Neuroradiol ISSN: 1591-0199 Impact factor: 1.610