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Paris-Trousseau syndrome : ウィキペディア英語版 | Paris-Trousseau syndrome
Paris-Trousseau syndrome (PTS) is an inherited disorder characterized by mild hemorrhagic tendency associated with 11q chromosome deletion. It manifests as a granular defect within an individual's platelets. It is characterized by thrombocytes with defects in α-granule components which affects the cell's surfeace area and, consequently, its abitlity to spread when necessary. ''FLI1'' has been suggested as a candidate. == See also ==
* Jacobsen syndrome
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