Juvenile Huntington Disease With Cerebellar-Predominant Atrophy Identified by Genome Sequencing
Enrique Gonzalez Saez-Diez1,2, Amy Tam1, Siofra Carty1
1Department of Neurology & F.M. Kirby Neurobiology Center, Movement Disorders Program, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Abstract:
Juvenile Huntington disease accounts for a small fraction of Huntington disease cases and is driven by the largest trinucleotide repeat expansions. We describe a 6-year-old boy with progressive global regression, generalized dystonia, and epilepsy, in whom serial imaging showed striking cerebellar-predominant atrophy with an initially normal-appearing striatum. Extensive metabolic testing, exome sequencing, and an ataxia repeat expansion panel were nondiagnostic. Research genome sequencing identified a large pathogenic huntingtin CAG repeat expansion that confirmatory testing sized beyond 180 repeats. This case illustrates a cerebellar-predominant imaging signature of extreme repeat expansions and the limitations of exome sequencing for detecting them.
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