COL4A1 Mutations Associated with a Characteristic Pattern of Intracranial Calcification

J. Livingston, D. Doherty, S. Orcesi, D. Tonduti, A. Piechiecchio, R. La Piana, E. Tournier-Lasserve, A. Majumdar, S. Tomkins, G. Rice, R. Kneen, M.S. van der Knaap, Y. Crow

    Research output: Contribution to JournalArticleAcademicpeer-review

    Abstract

    Introduction: Intracranial calcification (ICC) is a relatively common radiological finding in children undergoing investigation for neurological disorders. Many causes are recognised, and ICC is often regarded as a non-specific sign. Methods: From an ongoing study of ICC, we identified 5 patients with characteristic radiological features, in whom a mutation in the COL4A1 gene was found. Results: All patients had CT and MR imaging. MR images demonstrated features of periventricular leukomalacia with irregular dilatation of the lateral ventricles with or without porencephaly, loss of hemispheric white matter volume, and high signal on T2 and FLAIR sequences within periventricular and deep white matter. Calcification was apparent on MR in 4 patients. CT scans demonstrated spot and linear calcification in the subependymal region and around areas of porencephaly. Calcification was also visible in the deep cerebral white matter and basal ganglia. 1 patient showed calcification in the central pons. Conclusion: ICC occurs in COL4A1-related disease. The radiological features are distinct from other conditions demonstrating recognisable patterns of ICC, such as congenital cytomegalovirus infection and Aicardi-Goutires syndrome. In the absence of a known risk factor for periventricular leukomalacia, the presence of these radiological findings should suggest the possibility of COL4A1-related disease. © Georg Thieme Verlag KG Stuttgart - New York.
    Original languageEnglish
    Pages (from-to)227-233
    JournalNeuropediatrics
    Volume42
    Issue number6
    DOIs
    Publication statusPublished - 2011

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