Format

Send to

Choose Destination
Brain Dev. 2016 Jun;38(6):597-600. doi: 10.1016/j.braindev.2015.12.011. Epub 2016 Feb 8.

Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation.

Author information

1
Department of Pediatrics, Juntendo University, Faculty of Medicine, Japan. Electronic address: aigara@juntendo.ac.jp.
2
Department of Pediatrics, Aichi Medical University, Japan.
3
Tokyo Women's Medical University, Institute for Integrated Medical Sciences, Japan.
4
Department of Pediatrics, Juntendo University, Faculty of Medicine, Japan.

Abstract

We describe a girl with Down syndrome who experienced focal seizures and epileptic spasms during infancy. The patient was diagnosed as having trisomy 21 during the neonatal period. She had focal seizures at five months of age, which were controlled with phenobarbital. However, epileptic spasms appeared at seven months of age in association with hypsarrhythmia. Upon treatment with adrenocorticotropic hormone, her epileptic spasms disappeared. Her younger brother also had focal seizures at five months of age. His development and interictal electroencephalogram were normal. The patient's father had had infantile epilepsy and paroxysmal kinesigenic dyskinesia. We performed a mutation analysis of the PRRT2 gene and found a c.841T>C mutation in the present patient, her father, and in her younger brother. We hypothesized that the focal seizures in our patient were caused by the PRRT2 mutation, whereas the epileptic spasms were attributable to trisomy 21.

KEYWORDS:

Benign infantile epilepsy; Down syndrome; Epileptic spasms; PRRT2 mutation

PMID:
26867511
DOI:
10.1016/j.braindev.2015.12.011
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center