Familial Clustering of Antiphospholipid Syndrome
Asma Saadia1, Sana Haseeb Khan1, Muhammad Dilawar Khan1
1Department of Pathology, Shalamar Medical and Dental College, Lahore, Pakistan.
Abstract:
Antiphospholipid syndrome (APS) is a systemic autoimmune disease characterised by thrombosis (venous or arterial) and/or pregnancy-related complications. There is very scanty literature available regarding familial occurrence of APS worldwide and to the best of our knowledge, this important aspect has never been previously reported from Pakistan. We are presenting three patients of a Pakistani family who presented with thrombotic and pregnancy-related complications. Screening of the asymptomatic family members was also carried out. Knowledge about the familial occurrence of the disease is important not only for better management of such patients but also to emphasise the need for future studies to unveil its genetic basis.
More Related Videos
06:48Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
10:21Author Spotlight: Exploring the Role of Inflammation in the Co-occurrence of Primary Sjogren's Syndrome and Lung Adenocarcinoma
Published on: September 20, 2024
Related Concept Videos
Peripheral Artery Disease I: Introduction
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Atherosclerosis II: Clinical Manifestations and Diagnostic Tests
Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation
Amyloid Fibrils
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
