Figure 3.

Diagnostic approach for suspected cases of inherited platelet function disorders. BSS: Bernard-Soulier Syndrome; GPS: Gray Platelet Syndrome; GT: Glanzmann thrombasthenia; STD: Signaling transmission defect (deficiencies in enzymes, G-proteins, CalDAG-GEF1, other signaling proteins); Specific defects in platelet receptors P2Y12 (ADP), Tpa (TxA2) or glycoprotein VI (GPVI) (collagen); SS: Scott Syndrome; HPS: Hermansky-Pudlak Syndrome; CHS: Chediak-Higashi Syndrome; QS: Quebec Syndrome. EM: electron microscopy; LTA: light transmission aggregometry; U46619:TxA2 analog; CRP: collagen-related peptide; Figure 2: Figure 2.