Results 31 to 40 of about 118,635,816 (237)

Hemophilia A yang Didapat: Suatu Tinjauan tentang Diagnosis dan Manajemen

open access: yesWMJ (Warmadewa Medical Journal), 2017
Acquired hemophilia A (AHA) is a rare acquired bleeding disorder, an autoimmune disease characterized by autoantibody directed against factor VIII.
I Made Bakta
doaj   +1 more source

Literature review and clinical observation of acquired idiopathic hemophilia with a new missense mutation in the factor VIII gene (His2026Arg) [PDF]

open access: yesТерапевтический архив, 2018
The article provides review of possible mechanisms of inhibitor coagulopathies, in particular of acquired hemophilia A. This pathology is an extremely rare disease occurring in 1-2 cases in 1 million per year. In the present study we provide data for two
V I ERSHOV   +7 more
doaj   +1 more source

Acquired hemophilia A in a patient treated by Ginkgo‐dipyridamolum

open access: yesClinical Case Reports, 2017
Key Clinical Message Acquired hemophilia A might be caused by Ginkgo‐dipyridamolum especially by Ginkgo, and it was successfully treated with hemostasis and immune‐suppression therapy including methylprednisolone and cyclophosphamide.
Jinbo Liu   +5 more
doaj   +1 more source

Acquired hemophilia A secondary to rheumatoid arthritis [PDF]

open access: yes, 2022
Acquired hemophilia A (AHA) is a rare plasma diathesis. Unlike congenital hemophilia A, AHA occurs in both sexes and the incidence of the disease increases with age.
Palus, Damian; Department of Hyper tension and Diabetology, Faculty of Medicine, Medical Univer sity of Gdańsk, Gdańsk, Poland   +13 more
core   +1 more source

A perioperative uncontrollable bleeding in an elderly patient with acquired hemophilia A: a case report [PDF]

open access: yes, 2013
Acquired hemophilia A should be taken into account in the differential diagnosis of perioperative bleeding in patients without any apparent reason for activated partial thromboplastin time ...
Foresta, G   +13 more
core   +1 more source

Factor VIII-hydrolyzing IgG in acquired and congenital hemophilia

open access: yes, 2009
Anti-factor VIII (FVIII) inhibitory IgG may arise as alloantibodies to therapeutic FVIII in patients with congenital hemophilia A, or as autoantibodies to endogenous FVIII in individuals with acquired hemophilia.
Uda, Taizo   +35 more
core   +2 more sources

A Case of Acquired Hemophilia A and Congenital Hemophilia B

open access: yesCureus, 2022
Congenital hemophilia B is a rare, inherited X-linked bleeding disorder caused by a deficiency of factor IX (FIX). Acquired hemophilia A is a rare, acquired bleeding disorder which presents as new onset bleeding in older adults due to the development of autoantibodies against factor VIII (FVIII).
Fortier, Julia C   +4 more
openaire   +2 more sources

Hemophilia a genetic disorder: diagnosis, treatment and prognosis [PDF]

open access: yes, 2016
Hemophilia a genetic disorder with patient’s inability to stop bleeding. There are two main types of hemophilia, hemophiliaA due to not enough clotting factor VIII and hemophilia B due to not enough factor IX,and acquired hemophilia A(AHA) caused by ...
AM Sharifa   +5 more
core   +2 more sources

Acquired factor VIII deficiency in prostate adenocarcinoma presenting as multiple hematomas and hemarthrosis

open access: yesSAGE Open Medical Case Reports, 2020
Acquired hemophilia A or acquired factor VIII deficiency is a rare bleeding disorder due to the presence of autoantibodies to factor VIII. It has been associated with autoimmune conditions, certain medications, and malignancy. It has a high morbidity and
Akeem Lewis   +4 more
doaj   +1 more source

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