Systemic Lupus Erythematosus | Causes, Symptoms & Treatments
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can affect almost any organ system.
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can affect almost any organ system.
Gastric ulcers are defined as a break in the mucosal barrier of the stomach lining that penetrates through the muscularis mucosa and is larger than 5 mm in diameter.
Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency that is characterized by eczema, recurrent infections, and micro-thrombocytopenia.
Human immunodeficiency virus (HIV) is an enveloped retrovirus … There are four main stages of HIV infection.
Good’s syndrome is a rare adult-onset thymoma-related immunodeficiency with an unknown cause.
Acquired angioedema (AAE) is defined as a deficiency in the C1 esterase inhibitor.
It is a rare disorder characterized by recurring angioedema without urticaria that may be linked to lymphoproliferative disorders (LPD).
Rheumatoid arthritis is a progressive, chronic, and degenerative autoimmune inflammatory disease that is primarily characterized by synovitis.
Acute Pancreatitis (AP) is an acute pancreatic inflammatory disorder caused by intracellular activation of pancreatic digestive enzymes.
Pernicious anemia (PA) is an autoimmune condition with a multifactorial etiology that includes environmental and immunological factors.
Sickle cell anemia is an inherited condition of the globin chains that leads to hemolysis and chronic organ damage.
Aplastic anemia (AA) is the syndrome of chronic primary hematopoietic failure caused by injury, which results in decreased or absent hematopoietic precursors in the bone marrow and accompanying pancytopenia.
Diamond Blackfan anemia (DBA) is a form of congenital anemia that is characterized by pure red cell aplasia and is related to congenital bone abnormalities.