Primary Insulin-Like Growth Factor-1 Deficiency (PIGFD), also known as Laron syndrome or growth hormone insensitivity syndrome, is a rare congenital disorder characterized by the body's…
Primary hypogonadism is defined as testicular failure that results in inadequate production of testosterone and impaired spermatogenesis. When the etiology is orchitis—an inflammatory condition of…
Primary hypogonadism is a clinical condition characterized by impaired testicular function resulting in reduced testosterone production and/or impaired spermatogenesis. When this condition arises as a…
Primary Hyperoxaluria Type I (PH1) is a rare autosomal recessive genetic disorder characterized by the overproduction of oxalate, a metabolic end product that the body…
Primary genital syphilis represents the first stage of syphilis infection, caused by the spirochete bacterium Treponema pallidum. Characterized by the appearance of a painless genital…
Primary focal hyperhidrosis of the axilla is a chronic condition characterized by excessive underarm sweating that occurs without identifiable medical cause. Unlike secondary hyperhidrosis, which…
Primary dysbetalipoproteinemia, also known as type III hyperlipoproteinemia, is a rare genetic lipid metabolism disorder characterized by the improper clearance of remnant lipoproteins from the…
Primary Cutaneous Anaplastic Large Cell Lymphoma (PC-ALCL) is a distinct subtype of CD30-positive T-cell lymphoproliferative disorders, predominantly manifesting in the skin without systemic involvement at…
Primary biliary cholangitis (PBC), previously known as primary biliary cirrhosis, is a chronic autoimmune liver disease that primarily affects the bile ducts within the liver.…