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FV Leiden mutation in young women with protein S deficiency remains undetected. Our objective was to determine the prevalence of FV Leiden in young women with protein S deficiency. We analyzed the FV genotype in 13 patients (mean age = 17 years) with type I protein S deficiency defined by a functional test. Five patients with a history of thrombosis were homozygous for the FV Leiden mutation in the factor V gene (40%) whereas eight were heterozygous (60%). Of the five homozygous women, two had thrombosis at time of testing, and one was a heterozygous carrier. Although the FV Leiden mutation appears to be important in type I protein S deficiency, FV Leiden does not appear to be a major contributor to thrombosis in young women. UNPUBLISHED

UNITED STATES COURT OF APPEALS
FOR THE FOURTH CIRCUIT

No. 02-6110

HAROLD O’NEAL BROWN,

Petitioner – Appellant,

versus

THOMAS CORCORAN, Warden of Lee County Jail;
STATE OF SOUTH CAROLINA,

Respondents – App

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