Paris-Trousseau syndrome
| Paris-Trousseau syndrome | |
|---|---|
| Other names | Paris-Trousseau thrombocytopenia[1] |
Paris-Trousseau syndrome (PTS) is an inherited disorder characterized by mild hemorrhagic tendency associated with 11q chromosome deletion.[2][3] 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 surface area and, consequently, its ability to spread when necessary.[citation needed]
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