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
Immunosuppression after solid organ transplantation is complex. Over the past 50 years, the medical community has witnessed great advances in the care of patien
ResponderEliminarWomen have unique health issues. And some of the health issues that affect both men and women can affect women differently. Unique issues include pregnancy, men
We are a medical group of physicians and health professionals that specialize in gastrointestinal disorders, nutrition and digestive health
Weight loss can be intentional, such as from dieting and exercise, or unintentional and be a manifestation of illness. Weight loss can result from a decrease in
Blood pressure numbers of less than 120/80 mm Hg are considered within the normal range. If your results fall into this category, stick with heart-healthy habit