There was a higher rate of blood clots reported in individuals with PWS due to chromosome deletion, but this did not reach statistical significance compared to other groups (among deletion subtype 4.9% (21/433) recorded blood clots, among UPD subtype 1.4% (4/285) recorded blood clots, 0% (0/25) were recorded in the Imprinting subtype, and 5% recorded blood clots in the “Other”/Don’t Know group (7/140); p = 0.096).
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Thrombosis Risk History and D-dimer Levels in Asymptomatic Individuals with Prader-Willi Syndrome.
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