Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation

Meredith Golomb, Mark Heiny, Bhuwan P. Garg

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

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.

Original languageEnglish
Pages (from-to)753-755
Number of pages3
JournalJournal of Child Neurology
Volume22
Issue number6
DOIs
StatePublished - Jun 2007

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Methylenetetrahydrofolate Reductase (NADPH2)
Plasminogen Activator Inhibitor 1
Stroke
Mutation
factor V Leiden

Keywords

  • Stroke
  • Thrombophilia
  • Thrombosis

ASJC Scopus subject areas

  • Clinical Neurology
  • Pediatrics, Perinatology, and Child Health

Cite this

Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation. / Golomb, Meredith; Heiny, Mark; Garg, Bhuwan P.

In: Journal of Child Neurology, Vol. 22, No. 6, 06.2007, p. 753-755.

Research output: Contribution to journalArticle

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