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Journal of Child Neurology
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Two Cousins With Neonatal Stroke, PAI-1 4G Variant and MTHFR A1298C Mutation

Meredith R. Golomb, MD, MSc

Division of Pediatric Neurology, Department of Neurology, Indiana University School of Medicine, Indianapolis, mgolomb{at}iupui.edu

Mark Heiny, MD, PhD

Division of Pediatric Hematology-Oncology Indiana University School of Medicine, Indianapolis

Bhuwan P. Garg, MBBS

Division of Pediatric Neurology, Department of Neurology, Indiana University School of Medicine, Indianapolis

The authors describe 2 female cousins with neonatal stroke. One was heterozygous for the plasminogen activator inhibitor-1 4G variant and compound heterozygous for the A1298C and C677T methylenetetrahydrofolate reductase mutations. Her cousin was homozygous for the plasminogen activator inhibitor-1 4G variant and heterozygous for the methylenetetrahydrofolate reductase A1298C and factor V Leiden mutations.

Key Words: thrombosis • thrombophilia • stroke

Journal of Child Neurology, Vol. 22, No. 6, 753-755 (2007)
DOI: 10.1177/0883073807304001
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