DAVID B. CRANE, Robert H. Hackler, LYMAN M. FISCHER
Abstract
A 21-year-old blond, white woman was evaluated for recurrent episodes of significant painless gross hematuria. She was found to have sickle cell trait, and hematologic evaluation made through four generations isolated the trait to the paternal side.
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A 21-year-old blond, white woman was evaluated for recurrent episodes of significant painless gross hematuria. She was found to have sickle cell trait, and hematologic evaluation made through four generations isolated the trait to the paternal side.
Key concepts: Medicine, Sickle cell trait, Gross hematuria, Trait, White (mutation), Internal medicine, Pediatrics, Surgery