Directory
Ringworm
Ringworm is an infectious disease caused by dermatophytes that affects the skin, hair, and nails. The disease manifests itself as...
Renal vein thrombosis
Renal vein thrombosis (RVT) is a pathological condition characterized by the formation of a blood clot in the renal vein, which leads to a disruption of...
Raynaud's phenomenon
Raynaud's phenomenon is a vasospastic reaction that results in temporary occlusion of peripheral arteries, usually in the fingers...
Rasmussen's encephalitis
Rasmussen's encephalitis is a rare but severe neurological disorder characterized by chronic inflammation of one or more of the...
Rectocele
Rectocele is a pathology characterized by protrusion of the rectal wall into the vaginal area, which is caused by weakening of...
Disaccharide conversion syndrome-SRD5A3-CDG
SRD5A3-CDG (SRD5A3-associated disaccharide conversion syndrome) is a rare genetic disorder related to ...
Transposition of internal organs - Situs Inversus
Situs inversus is a rare congenital disorder in which the arrangement of organs in the human body is mirrored...
Spinal cord abscess
A spinal cord abscess is a localized cavity filled with pus that forms within the spinal cord or its membranes.
Sebaceous gland adenoma
Adenoma of the sebaceous gland is a benign tumor that arises from the cells of the sebaceous glands, which are a component of the...
Aneurysm of the sinus of Valsalva
Aneurysm of the sinus of Valsalva is a pathological dilation of the sinus of Valsalva, located in the region of the aortic root. It is a...
Sandhoff's disease
Sandhoff disease is a rare inherited disorder that belongs to the group of lysosomal storage diseases...
Sutton's disease 2
Sutton's disease, also known as chronic target nephritis or chronic prostatitis, is an autoimmune disease...
Schindler's disease
Schindler's disease, also known as Schindler's syndrome, is a rare inherited disorder that belongs to the group of lipidoses. It...
Sialic acid storage disease
Sialic acid storage disease, also known as sialosis, is a rare genetic disorder caused by a defect in the...
Sunken fontanelles
Sunken fontanelles (or hypertensive sinus disease) are a condition characterized by the indentation (sinking) of the fontanelles...
Congenital spondyloepiphyseal dysplasia
Congenital spondyloepiphyseal dysplasia (CSD) is a rare genetic disorder that belongs to the group of bone dysplasias...
Secondary adrenal insufficiency
Secondary adrenal insufficiency (SAI) is a condition characterized by insufficient production of corticosteroids...
Secondary immunodeficiency (SID)
Secondary immunodeficiency (SID) is a condition in which the immune system is weakened due to various factors, such as...
Secondary Parkinsonism
Secondary parkinsonism is a syndrome that manifests itself with symptoms similar to Parkinson's disease, but has a high degree of secondary...
Secondary peritonitis
Secondary peritonitis is an acute inflammation of the abdominal cavity caused by an infection that occurs as a result of penetration...
Secondary systemic amyloidosis
Secondary systemic amyloidosis (SA) is a complex and potentially debilitating disorder characterized by deposition of amyloid...
Heterotopia of subcortical stripes
Heterotopia of the subcortical bands is a neurological condition characterized by abnormal arrangement of neural tissue, c...
Sea green histiocytosis
Sea-green histiocytosis (SCH) is a rare disorder characterized by abnormal proliferation of histiocytes that in...
Granuloma in the pool - Mycobacterium marinum
Mycobacterium marinum granuloma is a rare skin infection caused by a non-ubiquitous bacteria...
Stargardt's macular degeneration
Stargardt macular degeneration (SMD) is an inherited disorder of the retina that is characterized by progressive...
Short-chain acyl-CoA dehydrogenase deficiency
Short-chain acyl-CoA dehydrogenase (SCADA) deficiency is a rare inherited metabolic disorder caused by...
Succinyl-CoA:3-keto acid CoA transferase deficiency
Succinyl-CoA:3-ketoacid CoA transferase deficiency is a rare inherited disorder that belongs to a group of disorders of the...
Sulfite oxidase deficiency
Sulfite oxidase deficiency, or sulfite oxidase deficiency syndrome, is a rare genetic disorder caused by a lack of...
Succinic semialdehyde dehydrogenase deficiency
Succinic semialdehyde dehydrogenase deficiency (SSDH) is a rare inherited disorder that involves abnormal fat metabolism...
Sprengel's deformation
Sprengel's deformity is a developmental anomaly characterized by abnormal positioning and deformation of the scapula, in most cases...
