COAGULAÇAO
Informaçao geral
Directorios
Textos





Genetica da coagulação
Informaçao especializada
Activador do plasminogenio tecidular

Deficiencia em activador do plasminogenio
Ver inibidores da actividade do
plasminogenio
Agregaçao plaquetaria

Antiplasmina ( inibidor da plasmina)

Antitrombina

Deficiencia em antitrombina
Bernard- Soulier
Bradiquinina
Receptor da bradiquinina
Buerger
Ver trombangeite obliterante
Calicreina

Christmas
Deficiência do factor Christmas
– hemofilis B
Coagulaçao e gravidez

Coagulaçao intravascular
disseminada

Cofactor II da heparina
Dermatite purpúrica pigmentada


Fibrina


Factores da coagulaçso

FACTOR
|
NAME
|
SOURCE
|
PATHWAY
|
I
|
Fibrinogen
|
Liver
|
Common
|
II
|
Prothrombin (enzyme)
|
Liver *
|
Common
|
III
|
Thromboplastin
|
Released by damaged cells
|
Extrinsic
|
III
|
Thromboplastin
|
Released by platelets
|
Intrinsic
|
IV
|
Calcium ions
|
Bone and gut
|
Entire process
|
V
|
Proaccererin
(heat labile cofactor) |
Liver and Platelets
|
Extrinsic and Intrinsic
|
VII
|
Proconvertin (enzyme)
|
Liver *
|
Extrinsic
|
VIII
|
Anti-hemolytic factor(cofactor)
|
Platelets and endothelium
|
Intrinsic
|
IX
|
Christmas factor(plasma
thromboplastin component)
|
Liver *
|
Intrinsic
|
X
|
Stuart Prower factor (enzyme)
|
Liver *
|
Extrinsic and Intrinsic
|
XI
|
Plasma thromboplastin antecedent (enzyme)
|
Liver
|
Intrinsic
|
XII
|
Hageman
factor
|
Liver
|
Intrinsic; also activates plasmin
|
XIII
|
Fibrin stabilizing factor
|
Liver
|
Retards fibrinolysis
|
*vitamin K dependente
Factor III, factor tecidular ou
tromboplastina
https://en.wikipedia.org/wiki/Tissue_factor
Deficiencia em factor III
Factor IV
Factor V (Leiden)
Deficiencia em fsactor V
Trombofilia do factor V
Ver TROMBOFILIS
Factor VII ou proconvertina
Deficiencia em factor VII
Factor VIIa
Factor VIII

Deficiencia do factor VIII
Factor VIII aumentado
Factor IX ( Christmas)
.Ver CHRISTMAS
Factor X ( Stuart –
Power)

Deficiencia em factor X
Factor Xa
Factor XI

Drficiencia em factor XI
Factor XII ( Hageman)


Deficiencia em factor XII
Factor XIII


Deficiencia bem factor XIII
Fibrinogenio



Deficiencia em fibrinogenio
Fibrinolise

Hemofilia
·
Haemophilia A is a recessive X-linked genetic disorder involving a
lack of functional clotting Factor VIII and represents 80% of haemophilia
cases.
·
Haemophilia B is a recessive X-linked genetic disorder involving a
lack of functional clotting Factor IX. It comprises approximately 20%
of haemophilia cases.[11]
·
Haemophilia C is an autosomal genetic disorder (i.e. not X-linked) involving a lack of
functional clotting Factor XI. Haemophilia C is not completely recessive, asheterozygous individuals also show increased bleeding.[12]

Hipercoagulaçao

Homocistinemia e coagulação
Inibidor da plasmina (antiplasmina)

Deficiencia da antiplasmina
Inibidores da via do factor tecidular

Alfa 2 Macroglobulina

Deficiencia em alfa2 macroglobulina
May- Hegglin

Plaquetas


Plasmina

Plasminogenio
Activaçao do plasminogenio


Deficiencia em plasminogenio
Inibidor do activador do plasminogenio

Pre-calicreina
Deficiencia em pre-calicreina
Proteinas C e S

Deficiencia em proteínas C
Deficiencia congénita em proteínas C e S
Deficiencia em proteína S
Proteina Z
Deficiencia em proteína Z
Protrombina

Deficiencia em protrombina
Mutaçao do gene da protrombina
Tempo de protrombina
Purpura
Purpura actínica

Purpura de Bateman ou purpura senil

Purpura fulminans

Purpura de Henoch- Schonlein

https://en.wikipedia.org/wiki/Henoch%E2%80%93Sch%C3%B6nlein_purpura


http://www.webmd.com/skin-problems-and-treatments/henoch-schonlein-purpura-causes-symptoms-treatment
Purpura de Henoch-Schonlein associada
doença de Graves
Purpura trombocitogenica idiopática
http://www.netdoctor.co.uk/conditions/heart-and-blood/a1176/idiopathic-thrombocytopenic-purpura-itp/

Purpura trombocitopénica imune
Purpura trombocitopénica trombótica
Quininogenio de alto
peso molecular
Deficiencia do quininogenio de alto peso molecular~
Sindroma de anticorpos antifosfolipidos
Terapia trombolitica
Trombangeite
obliterante ou doença de Buerger


Trombastenia de
Glanzman
Trombina



Trombocitopenia
http://www.netdoctor.co.uk/conditions/heart-and-blood/a1177/thrombocytopenia-reduced-platelet-count/

Plaquetaferese
Transfusao de plaquetas
Trombo


Trombocitopenia autoimune
Trombocitopenia
induzida pela heparina

Trombocitose
Trombocitose essencial

Trombocitose secundaria

Trombofilia

Trombolise dirigida por
catetero
Trombomodulina
Trombopoietina

Trombose
Trombose da artéria
basilar
Trombose coronária

Trombose portal
Budd – Chiari
http://www.chp.edu/our-services/transplant/liver/education/liver-disease-states/budd-chiari-syndrome
Trombose das veias
profundas

Trombose venosa
cerebral



Uroquinase

Von Willebrandt