4q21 microdeletion in a patient with epilepsy and brain malformations

Am J Med Genet A. 2015 Jun;167(6):1409-13. doi: 10.1002/ajmg.a.36910. Epub 2015 Apr 2.

Authors

Sho Yano^{1

2}, Meredithe McNamara², Sara Halbach³, Darrel Waggoner^{2

3}

Affiliations

¹ Section of Pediatric Neurology, Department of Pediatrics, University of Chicago Comer Children's Hospital, Chicago, Illinios.
² Department of Pediatrics, University of Chicago Comer Children's Hospital, Chicago, Illinios.
³ Department of Human Genetics, University of Chicago, Chicago, Illinios.

PMID: 25847229
DOI: 10.1002/ajmg.a.36910

No abstract available

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / genetics*
Abnormalities, Multiple / pathology
Child, Preschool
Chromosome Deletion
Chromosome Disorders / genetics*
Chromosome Disorders / pathology
Chromosomes, Human, Pair 4 / genetics
Epilepsy / genetics*
Epilepsy / pathology
Humans
Male
Malformations of Cortical Development / genetics*
Malformations of Cortical Development / pathology
Seizures / genetics*
Seizures / pathology

Supplementary concepts

Chromosome 4q- Syndrome