Results 11 to 20 of about 548 (135)
Primary antiphospholipid syndrome presenting with homonymous quadrantanopsia
Purpose: To report a case of primary antiphospholipid syndrome presenting with isolated homonymous superior quadrantanopsia. Observations: A 50-year-old Korean man presented with subjective visual disturbance for 1 month.
Hee Kyung Yang +4 more
doaj +1 more source
Catastrophic antiphospholipid syndrome presenting as fever of unknown origin
Antiphospholipid syndrome is characterized by the presence of antiphospholipid antibodies with characteristic clinical manifestation, which include venous, arterial thrombosis, thrombotic microangiopathy, and recurrent fetal loss.
Fatma I Al-Beladi
doaj +1 more source
RETROSPECTIVE ANALYSIS OF MEDICAL CHARTS OF PATIENTS WITH ANTIPHOSPHOLIPID SYNDROME
Background. Antiphospholipid attracts the attention of clinicians in various fields of medicine. This pathology is characterized by a triad of clinical and laboratory signs: recurrent venous or arterial thrombosis with localization in any part of the ...
V. I. Savytskyi
doaj +1 more source
Homonymous hemianopia in the primary antiphospholipid syndrome [PDF]
A woman aged 26 years was referred by her GP to the eye casualty department with sudden-onset left homonymous hemianopia and right-sided headache. Full ophthalmic examination was normal with the exception of a left homonymous hemianopia confirmed with automated perimetry.
Derek Kwun-Hong, Ho +3 more
openaire +2 more sources
Antiphospholipid Syndrome: A Review
Antiphospholipid syndrome (APS) is an autoimmune disease characterized by venous thromboembolism, arterial thrombosis, and obstetric morbidities in the setting of persistently positive levels of antiphospholipid antibodies.
Md. Motahar Hossain +3 more
doaj +1 more source
Retinal ischemia as the first manifestation of antiphospholipid antibody syndrome [PDF]
Antiphospholipid antibody syndrome (APS) is characterized by the development of venous and/or arterial thrombosis and by gestational morbidity (recurrent fetal losses) in the presence of antiphospholipid antibodies.
Giovanna Maria Oliveira Ribeiro +3 more
doaj +1 more source
A Rare Presentation of Primary Antiphospholipid Syndrome [PDF]
This case presents a young patient with myocardial infarction, in-situ thrombosis of left anterior descending coronary artery and right common-iliac artery due to primary antiphospholipid syndrome. This report discusses the relationship between antiphospholipid antibodies and coronary artery disease along with management of this rare condition.
Panduranga, Prashanth +2 more
openaire +2 more sources
Primary Adrenal Failure due to Antiphospholipid Syndrome
Background. Antiphospholipid syndrome (APS) characterized by thrombosis and abortus may rarely cause primary adrenal failure. Case Presentations. A 34-year-old male presented with hypotension, hypoglycemia, hyperpigmentation on his skin and oral mucosa ...
Murat Sahin +6 more
doaj +1 more source
Background Antiphospholipid syndrome is an autoimmune disorder characterized by the presence of antiphospholipid antibodies and commonly presents with vascular thromboembolic phenomena, thrombocytopenia, and obstetric complications.
Yogesh Sharma +2 more
doaj +1 more source
Antiphospholipid syndrome is a rare disorder. Acute myocardial infarction is uncommon among these patients. Here we report a case of a 44-year-old man with antiphospholipid syndrome admitted for acute inferior myocardial infarction.
Serdar Biceroglu +4 more
doaj +1 more source

