Periventricular nodular heterotopia and dystonia due to an ARFGEF2 mutation.

Abstract

BACKGROUND:

Heterotopias are a neuronal migration disorder caused by extrinsic factors or by genetic mutations. When the location is periventricular, the most frequent genetic cause is the mutation in the "filamin A2 gene", which is X-linked. New genes for periventricular nodular heterotopia with an autosomal inheritance pattern have been recently discovered.

PATIENTS:

We describe two siblings. The girl, who was prenatally diagnosed ventriculomegaly, had delayed development. At 6 months, she had no head control and variable muscle tone, alternating low axial tone with jerking movements. She became microcephalic. Magnetic resonance imaging at 12 months of age revealed enlarged lateral ventricles, periventricular nodular heterotopia, thin corpus callosum, a T2-hyperintensity of the putamen and the thalamus, and a loss of volume of lenticular nucleus. At 18 months, she developed sporadic myoclonic seizures that were well controlled with valproic acid. Her younger brother also developed progressive microcephaly and psychomotor delay by 6 months. He exhibited axial hypotonia with a prominent dystonic-athetoid component. Magnetic resonance imaging at 15 months of age revealed asymmetric ventriculomegaly plus diffuse nodules lining the temporal horns, a thin corpus callosum, and hyperintensity signal in putamens. He had no seizures.

RESULTS:

Because of the association of microcephaly, developmental delay with dystonic movements, the imaging results, and the probable autosomal recessive inheritance pattern, genetic analysis was requested. This detected a homozygous nonsense mutation in ARFGEF2 gene, at the DNA level c.388C>T in exon 4.

CONCLUSIONS:

The presence of dyskinetic movements in individuals with acquired microcephaly could be a manifestation of periventricular nodular heterotopia due to ARFGEF2 mutation.

• Authors: Eduardo Jesús Bardón-Cancho, Lucía Muñoz-Jiménez, María Vázquez-López, Yolanda Ruíz-Martín, Marina García-Morín, Estíbaliz Barredo-Valderrama
• Journal: Pediatric neurology (Pediatr Neurol) Vol. 51 Issue 3 Pg. 461-4 (Sep 2014) ISSN: 1873-5150 [Electronic] United States
• PMID: 25160555 (Publication Type: Case Reports, Journal Article)
• Copyright: Copyright © 2014 Elsevier Inc. All rights reserved.

Chemical References

• ARFGEF2 protein, human
• Codon, Nonsense
• Guanine Nucleotide Exchange Factors

Topics

• Brain (pathology)
• Codon, Nonsense
• DNA Mutational Analysis
• Diagnosis, Differential
• Dystonic Disorders (diagnosis, genetics, pathology)
• Female
• Guanine Nucleotide Exchange Factors (genetics)
• Humans
• Infant
• Magnetic Resonance Imaging
• Male
• Periventricular Nodular Heterotopia (diagnosis, genetics, pathology)
• Siblings