Directory
Triple X syndrome
Triple X syndrome (also known as 47,XXX syndrome) is a genetic condition caused by the presence of an extra X...
Thrombocytopenia and absent radius syndrome
Thrombocytopenia-absent radius (TAR) syndrome is a rare genetic disorder characterized by a combination of thrombocytopenia...
Tethered Cord Syndrome
Tethered cord syndrome is a rare disorder characterized by abnormal spinal or nerve tethering...
Tetanus
Tetanus is an acute infectious toxic disease caused by Clostridium tetani, an anaerobic bacterium capable of producing...
Tabes
Spinal cord paralysis, or spinal cord tabes, is an acute infectious disease caused by the polio virus...
T-cell lymphoma
T-cell lymphoma (TCL) is a malignancy that arises from T lymphocytes, which are key to...
Thalassemia
Thalassemia is a genetic disorder characterized by a disorder in the synthesis of globin, one of the main proteins that is part of...
Thanatophoric dysplasia
Thanatophoric dysplasia (TD) is a severe hereditary disease belonging to the group of constitutional dysplasias...
Telangiectasia
Telangiectasia is an abnormal dilation of small blood vessels, usually capillaries, that appears on the surface of the skin...
Tendinitis
Tendinitis, or inflammation of the tendons, is a clinical condition characterized by pain and limited mobility.
Tenesmus
Tenesmus is a painful condition characterized by a sensation of sharp pain in the abdominal area, especially in the lower t...
Tenosynovitis
Tenosynovitis is an inflammatory disease that affects the tendon sheaths, which are the structures that wrap around the tendons...
Teratocarcinosarcoma
Teratocarcinosarcoma (TCS) is a rare and aggressive form of tumor characterized by the presence of both carcinoma and...
Teratoma of the mediastinum
A mediastinal teratoma is a rare tumor-like formation that forms in the mediastinum, that is, in the chest area, located...
Tetralogy of Fallot
Tetralogy of Fallot is a congenital heart defect that is caused by the presence of four characteristic anatomical anomalies: stenosis...
Tetrasomy 9p
Tetrasomy 9p (9p tetrasomy) is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 9.
Tetrasomy X
Tetrasomy X, also known as 49,XXXX syndrome, is a genetic disorder characterized by the presence of four extra...
Thymic epithelial tumor
Thymic epithelial tumor (TET) is a rare type of tumor that arises from the glandular cells of the thymus, the organ responsible for ...
Thyroid storm
Thyroid storm is a severe and acute condition that occurs when the level of thyroid hormones in the blood increases sharply, causing...
Thyrotoxic periodic paralysis
Thyrotoxic periodic paralysis (TPP) is a rare but serious disorder characterized by hypercapnia, muscle weakness...
Tyrosinemia type 2
Tyrosinemia type 2 (T2) is a rare inherited metabolic disorder caused by a deficiency of the enzyme responsible for...
Tyrosinemia type 1
Tyrosinemia type 1 (TT1) is a rare genetic metabolic disorder associated with impaired tyrosine metabolism. This disease...
Tyrosinemia type 3
Tyrosinemia type 3 is a rare genetic disorder that belongs to a group of amino acid metabolism disorders associated with abnormal me...
Typhus
Typhus is an infectious disease caused by various types of salmonella, the most well-known of which is...
Toxic Megacolon
Toxic megacolon is a serious complication of various diseases that occurs as a result of a significant expansion of the colon...
Toxic synovitis
Toxic synovitis is damage to the synovial membrane of the joints caused by exposure to various toxic agents...
Toxic nodular goiter
Toxic nodular goiter (TNG) is a thyroid disorder characterized by the formation of one or more nodules in the tissue...
Tomacular neuropathy
Tomacular neuropathy is a rare but serious disorder characterized by degeneration of a thin layer of nerve tissue located...
Tonsillitis
Tonsillitis is an inflammatory condition that affects the tonsils, located at the back of the throat. The condition can be acute or...
Hirschsprung's disease - Colonic aganglionosis
Hirschsprung disease, also known as colonic aganglionosis, is a congenital disorder associated with the absence of nerves...
