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Periventricular Heterotopia in Common Microdeletion Syndromes

By M. van Kogelenberg, S. Ghedia, G. McGillivray, D. Bruno, R. Leventer, K. MacDermot, J. Nelson, L. Nagarajan, J.A. Veltman, A.P. de Brouwer, R.J. McKinlay Gardner, H. van Bokhoven, E.P. Kirk and S.P. Robertson

Abstract

Periventricular heterotopia (PH) is a brain malformation characterised by heterotopic nodules of neurons lining the walls of the cerebral ventricles. Mutations in FLNA account for 20–24% of instances but a majority have no identifiable genetic aetiology. Often the co-occurrence of PH with a chromosomal anomaly is used to infer a new locus for a Mendelian form of PH. This study reports four PH patients with three different microdeletion syndromes, each characterised by high-resolution genomic microarray. In three patients the deletions at 1p36 and 22q11 are conventional in size, whilst a fourth child had a deletion at 7q11.23 that was larger in extent than is typically seen in Williams syndrome. Although some instances of PH associated with chromosomal deletions could be attributed to the unmasking of a recessive allele or be indicative of more prevalent subclinical migrational anomalies, the rarity of PH in these three microdeletion syndromes and the description of other non-recurrent chromosomal defects do suggest that PH may be a manifestation of multiple different forms of chromosomal imbalance. In many, but possibly not all, instances the co-occurrence of PH with a chromosomal deletion is not necessarily indicative of uncharacterised underlying monogenic loci for this particular neuronal migrational anomaly

Topics: Original Article
Publisher: S. Karger AG
OAI identifier: oai:pubmedcentral.nih.gov:2883850
Provided by: PubMed Central
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