Category: Tipuri de hemofilie

Tratamentul hemofiliei A

Tratamentul pe tot parcursul vieții este necesar pentru persoanele cu hemofilie A pentru a înlocui factorul de coagulare lipsă în sângele lor.

Hemofilia tip A

Hemofilia A (hemofilia clasica), cauzata de deficienta activitatii coagulante a FVIII, reprezinta, ca frecventa, cea de-a doua boala hemoragica mostenita dupa boala von Willebrand, cu o incidenta de pana la 1/10000 persoane, cu o prevalenta similara intre diferitele grupe rasiale.

Hemofilia tip B

Hemofilia B (boala Christmas) este caracterizată prin deficiența activității coagulante a FIX....

Boala von Willebrand

Boala von Willebrand reprezintă cea mai frecventă coagulopatie ereditară (moștenită) ce se caracterizează prin apariția unor sângerări recurente.

Alte deficiențe de coagulare

Sunt afecțiuni în care există un deficit de sinteză, cantitativ sau calitativ, al unuia din factorii de coagulare: I, II, V, VII, X, XI, sau XIII.

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