Feb 25, 2026
Eisenmenger Syndrome represents the most advanced and irreversible stage of pulmonary hypertension caused by congenital heart disease. It occurs when
Feb 25, 2026
Congestive hepatopathy represents a spectrum of liver dysfunction resulting from elevated systemic venous pressure, primarily due to right-sided heart failure
Feb 23, 2026
Hypophosphatemic rickets (HR) represents a group of rare genetic and acquired disorders characterized by impaired renal phosphate reabsorption, leading to
Feb 23, 2026
Familial Adenomatous Polyposis (FAP) is a rare, inherited colorectal cancer syndrome characterized by the development of hundreds to thousands of
Feb 22, 2026
Pseudoxanthoma Elasticum (PXE) is a rare, inherited multi-system disorder characterized by the progressive mineralization and fragmentation of elastic fibers in
Feb 22, 2026
Hereditary Hemorrhagic Telangiectasia (HHT), historically known as Osler-Weber-Rendu syndrome, is a complex autosomal dominant genetic disorder characterized by abnormal blood
Feb 21, 2026
Rett Syndrome is a rare, neurodevelopmental disorder that primarily affects females and is characterized by a period of normal early
Feb 21, 2026
Thromboangiitis Obliterans (TAO), often referred to as Buerger’s disease, is a rare, non-atherosclerotic inflammatory vasculopathy primarily affecting the small and
Feb 20, 2026
Temporomandibular disorders (TMD) represent a broad spectrum of clinical problems involving the masticatory muscles, the temporomandibular joint (TMJ), and associated
Feb 20, 2026
Paget Disease of Bone (PDB), medically known as osteitis deformans, is a chronic skeletal disorder characterized by excessive and disorganized
Feb 18, 2026
Anti-Glomerular Basement Membrane (Anti-GBM) disease is a rare but life-threatening autoimmune disorder characterized by the presence of autoantibodies directed against
Feb 18, 2026
Otic barotrauma, commonly known as ear barotrauma or aerotitis media, represents a physical injury to the ear, most frequently the
Feb 16, 2026
Budd-Chiari Syndrome (BCS) is a rare and complex vascular disorder of the liver characterized by the obstruction of the hepatic
Feb 15, 2026
Angioedema is a distinct, self-limiting, but potentially life-threatening clinical condition characterized by rapid, non-pitting swelling of the deeper layers of
Feb 15, 2026
Subacute Sclerosing Panencephalitis (SSPE) is a rare, progressive, and fatal neurological disorder that arises as a late complication of the
Feb 13, 2026
Medullary Sponge Kidney (MSK), also known as Cacchi-Ricci disease, is a benign congenital renal anomaly characterized by cystic dilatation of
Feb 11, 2026
Fragile X Syndrome (FXS) represents the most common inherited cause of intellectual disability and the most frequent single-gene cause of
Feb 10, 2026
Pure Red Blood Cell Aplasia (PRCA) is a rare hematologic disorder characterized by a selective absence of erythroid precursors in
Feb 9, 2026
Necrotizing Soft-Tissue Infection (NSTI) represents one of the most critical and rapidly progressive emergencies in clinical medicine. Often referred to
Jan 27, 2026
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a rare, severe autoimmune demyelinating disease of the central nervous system (CNS) that primarily
Jan 24, 2026
Arthrogryposis Multiplex Congenita (AMC) represents a non-progressive, congenital condition characterized by multiple joint contractures present at birth. The term derives
Jan 24, 2026
Hutchinson-Gilford Progeria Syndrome (HGPS), commonly known as Progeria, is an extremely rare, fatal genetic condition characterized by rapid, premature aging
Jan 24, 2026
Fibrillary glomerulopathy (FG) and immunotactoid glomerulopathy (ITG) are rare, distinct forms of glomerular diseases characterized by the deposition of organized
Jan 24, 2026
Arginine Vasopressin Resistance (AVR), commonly known as Nephrogenic Diabetes Insipidus (NDI), is a complex disorder of water balance characterized by
Jan 21, 2026
Small Intestinal Bacterial Overgrowth (SIBO) is a clinical condition characterized by an excessive proliferation of bacteria in the small intestine.
Jan 21, 2026
Hereditary Cryopyrin-Associated Periodic Syndromes (CAPS) represent a spectrum of rare, autoinflammatory disorders driven by mutations in the NLRP3 gene. This group
Jan 21, 2026
Hypereosinophilic syndrome (HES) represents a diverse group of rare hematologic disorders characterized by a sustained, marked elevation of eosinophils in
Jan 13, 2026
Hypoplastic Left Heart Syndrome (HLHS) is one of the most complex and critical congenital heart defects (CHDs) presenting in the
Jan 13, 2026
Protein C deficiency is a rare, inherited hematological disorder that significantly increases an individual’s risk of developing abnormal blood clots,
Jan 13, 2026
Therapeutic apheresis (TA) is a specialized extracorporeal therapy where blood is drawn from a patient, separated into its components (plasma,
Jan 12, 2026
Persistent Truncus Arteriosus (PTA) is a rare and critical congenital heart defect (CHD) characterized by a single arterial vessel arising
Jan 12, 2026
Vaginitis, an inflammation of the vagina, is one of the most common reasons for women to seek gynecological care. While
Jan 12, 2026
Cervicitis is a prevalent gynecological condition characterized by inflammation of the cervix, the lower part of the uterus that connects
Jan 11, 2026
Total Anomalous Pulmonary Venous Return (TAPVR) is a critical congenital heart defect (CHD) characterized by the abnormal connection of the
Jan 11, 2026
Candidal vaginitis, commonly known as a yeast infection, is one of the most frequent reasons for women to seek gynecological
Jan 11, 2026
Cervical mucus is a complex biological fluid secreted by the endocervical glands that plays a pivotal role in female reproductive
Jan 10, 2026
Vaginal prolapse is a common and often under-discussed gynecological condition characterized by the descent of the vaginal walls. It occurs
Jan 10, 2026
The transition from intrauterine to extrauterine life is a period of profound physiological adaptation for the newborn. While many infants
Jan 8, 2026
Pregnancy is a unique physiological state characterized by profound adaptations to support the developing fetus. While these changes are essential
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