La hemofilia es un problema hemorrágico. Las personas con hemofilia no sangran más rápido que lo normal, pero pueden sangrar durante un período más prolongado. Su sangre no contiene una cantidad suficiente de factor de coagulación. El factor de coagulación es una proteína en la sangre que controla el sangrado. La hemofilia es bastante infrecuente. Aproximadamente 1 en 10.000 personas nace con ella.
Tipos de hemofilia
El tipo más común de hemofilia se llama hemofilia A. Esto quiere decir que la persona no tiene suficiente factor VIII (factor ocho).
Un tipo menos común es la denominada hemofilia B. Esta persona no tiene suficiente factor IX (factor nueve). El resultado es el mismo para la hemofilia A y B, o sea, un sangrado por un tiempo mayor que el normal. En personas con trastornos de la coagulación, el proceso de la coagulación no funciona adecuadamente. Por esta razón, las personas con trastornos de la coagulación pueden sangrar más tiempo de lo normal y algunas podrían presentar hemorragias espontáneas en las articulaciones, los músculos u otras partes del cuerpo.
La hemofilia es un trastorno de la coagulación que afecta a aproximadamente una de cada 10,000 personas. La sangre de las personas con hemofilia no tiene suficiente factor de coagulación VIII o IX. Debido a esto pueden sangrar más tiempo de lo normal. El trastorno de la coagulación más común es la enfermedad de von Willebrand (EVW). Por lo general es menos grave que otros trastornos de la coagulación. Muchas personas con EVW podrían no saber que padecen el trastorno porque sus síntomas hemorrágicos son muy leves.
Las deficiencias de factor poco comunes son trastornos en los que uno de diversos factores de la coagulación está ausente o no funciona adecuadamente.Los conocimientos sobre estos trastornos son menores porque se diagnostican muy rara vez; de hecho, muchos solo se descubrieron en los últimos 40 años.
Por último, los trastornos hereditarios de la función plaquetaria son padecimientos en los que las plaquetas no funcionan como debieran, lo que provoca una tendencia a hemorragias o moretones.
Hemophilia is a bleeding problem. People with hemophilia do not bleed faster than normal, but may bleed for a longer period. His blood does not contain a sufficient amount of clotting factor. The clotting factor is a protein in the blood that controls bleeding. Hemophilia is quite rare. About 1 in 10,000 people are born with it.
Types of hemophilia
The most common type of hemophilia is called hemophilia A. This means that the person does not have enough factor VIII (factor eight).
A less common type is called hemophilia B. This person does not have enough factor IX (factor nine). The result is the same for hemophilia A and B, ie, bleeding for longer than normal. In people with bleeding disorders, clotting process does not work properly. For this reason, people with bleeding disorders may bleed longer than normal and may present some spontaneous bleeding into joints, muscles or other body parts.
Hemophilia is a bleeding disorder that affects about one in 10,000 people. The blood of people with hemophilia do not have enough clotting factor VIII or IX. Because this may bleed longer than normal. The bleeding disorder is more common von Willebrand disease (VWD). It is usually less severe than other bleeding disorders. Many people with VWD may not know they have the disorder because its symptoms are very mild bleeding.
The rare factor deficiencies are disorders in which one of several clotting factors are missing or not working adecuadamente.Los knowledge about these disorders are under diagnosed because very rarely, in fact, many were discovered only in the last 40 years.
Finally, inherited disorders of platelet function are conditions in which platelets are not working as they should, causing a tendency to bleeding or bruising.
Hämophilie ist eine verstärkte Blutungsneigung. Menschen mit Hämophilie nicht schneller als normal bluten, kann aber für einen längeren Zeitraum zu bluten. Sein Blut nicht eine ausreichende Menge an Gerinnungsfaktor. Die Gerinnungszeit Faktor ist ein Protein im Blut, Blutungen kontrolliert. Hämophilie ist recht selten. Über 1 in 10.000 Menschen sind mit ihm geboren.
Arten der Hämophilie
Die häufigste Art der Hämophilie wird als Hämophilie A. Dies bedeutet, dass die Person nicht genug Faktor VIII (Faktor acht).
Eine weniger häufige Art wird als Hämophilie B. Diese Person hat nicht genug Faktor IX (Faktor neun). Das Ergebnis ist das gleiche für Hämophilie A und B, dh, Blutungen länger als normal. Bei Menschen mit Blutgerinnungsstörungen, bedeutet Blutgerinnung nicht richtig funktionieren. Aus diesem Grund können Menschen mit Blutgerinnungsstörungen länger als normal bluten und kann einige spontane Blutungen in Gelenken, Muskeln oder andere Körperteile zu präsentieren.
Hämophilie ist eine Blutgerinnungsstörung, die etwa eine von 10.000 Menschen betroffen sind. Das Blut von Menschen mit Hämophilie nicht genug Gerinnungsfaktor VIII oder IX. Denn dies kann länger als normal bluten. Die Blutungsneigung ist häufiger von Willebrand Krankheit (VWD). Es ist in der Regel weniger streng als andere Blutgerinnungsstörungen. Viele Menschen mit VWD nicht wissen, dass sie die Krankheit, weil die Symptome sehr mild Blutungen sind.
Die seltenen Faktor Mängel sind Erkrankungen, bei denen eine von mehreren Gerinnungsfaktoren fehlen oder nicht funktionieren adecuadamente.Los Wissen über diese Erkrankungen sind unter diagnostiziert, weil sehr selten, in der Tat, viele erst in den letzten 40 entdeckt wurden Jahren.
Schließlich Erbkrankheiten der Thrombozytenfunktion sind Bedingungen, unter denen Blutplättchen nicht arbeiten, wie sie sollten, was eine Tendenz zu Blutungen oder Blutergüsse.
L’hémophilie est un problème de saignement. Personnes atteintes d’hémophilie ne saignent pas plus vite que la normale, mais peuvent saigner pendant une longue période. Son sang ne contient pas une quantité suffisante de facteur de coagulation. Le facteur de coagulation est une protéine du sang qui contrôle des saignements. L’hémophilie est assez rare. Environ 1 sur 10.000 personnes sont nées avec elle.
Types d’hémophilie
Le type le plus commun de l’hémophilie est appelé hémophilie A. Cela signifie que la personne n’a pas suffisamment de facteur VIII (facteur huit).
Un type moins commun s’appelle hémophilie B. Cette personne n’a pas assez de facteur IX (facteur neuf). Le résultat est le même pour l’hémophilie A et B, c’est à dire, des saignements plus longs que la normale. Chez les personnes atteintes de troubles hémorragiques, processus de coagulation ne fonctionne pas correctement. Pour cette raison, les personnes ayant des troubles hémorragiques peuvent saigner plus que la normale et peuvent présenter des saignements spontanés dans les articulations, les muscles ou les autres parties du corps.
L’hémophilie est un trouble de la coagulation qui touche environ une personne sur 10.000 personnes. Le sang des personnes atteintes d’hémophilie n’ont pas assez de facteur de coagulation VIII ou IX. Parce que cela peut saigner plus que la normale. Le trouble de saignement est plus fréquente maladie de von Willebrand (VWD). Il est généralement moins sévère que d’autres troubles hémorragiques. Beaucoup de gens avec maladie de von Willebrand ne savent pas qu’ils ont la maladie car ses symptômes sont très légers saignements.
Les carences de facteur rares sont les troubles dans lesquels l’un des nombreux facteurs de coagulation sont manquantes ou inopérantes les connaissances adecuadamente.Los de ces troubles sont sous-diagnostiquées parce que très rarement, en fait, beaucoup ont découvert que dans les 40 derniers années.
Enfin, les troubles héréditaires de la fonction plaquettaire sont les conditions dans lesquelles les plaquettes ne fonctionnent pas comme ils le devraient, ce qui provoque une tendance aux saignements ou des ecchymoses.
FUENTE: FEDERACIÓN MUNDIAL DE LA HEMOFILIA / TRASOS 2013
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