Type 1 diabetes mellitus (T1D) is an autoimmune disorder characterized by the destruction of insulin-producing beta cells in the pancreas. The progression of T1D is…
Deficiency of Interleukin-1 Receptor Antagonist (DIRA) is an uncommon autoinflammatory disease resulting from autosomal recessive mutations in the IL1RN gene. This condition leads to unregulated…
Bile acid synthesis disorders (BASDs) are a group of rare genetic conditions characterized by defects in the enzymatic pathways responsible for bile acid production. These…
Peroxisomal disorders are a group of inherited metabolic diseases characterized by dysfunctional peroxisomes, cellular organelles essential for lipid metabolism, including bile acid synthesis. A deficiency…
Deep vein thrombosis (DVT) and pulmonary embolism (PE) are critical components of venous thromboembolism (VTE), a condition with significant morbidity and mortality. DVT involves the…
Deep vein thrombosis prevention is a serious condition characterized by the formation of blood clots in deep veins, predominantly in the legs. Preventing DVT is…