Alpha-1 Antitrypsin Deficiency (AAT deficiency) is a genetic condition that affects the levels of a protein in the body called Alpha-1...

Alkaptonuria is a rare genetic condition that affects how the body processes certain proteins. This disorder leads to a buildup of a...

Ectodermal dysplasia (ED) is a group of genetic disorders that affect the development of certain parts of the body, including the skin,...

Dermatofibrosarcoma protuberans (DFSP) is a rare type of skin cancer that typically starts in the middle layer of the skin called the...

Toxic megacolon is a serious health issue that occurs when the colon becomes extremely swollen and inflamed. This condition can be...

Prothrombin deficiency is a rare blood disorder that affects how well your blood can clot. It can lead to serious bleeding problems,...

Freeman-Sheldon Syndrome (FSS), often referred to as "whistling face syndrome," is a rare genetic condition that affects muscle...

Bronchiolitis is a common lung infection that primarily affects infants and young children. It occurs when the small air passages in the...

Benign Essential Tremor (BET) is a common nervous system disorder that causes involuntary shaking, especially in the hands. While not...

Oral lichen planus is a long-lasting condition that affects the inside of the mouth, causing discomfort and various symptoms. This...

Insulinoma is a rare type of tumor that forms in the pancreas. It produces too much insulin, which can lead to low blood sugar levels....

Hurler syndrome is a rare genetic disorder that falls under a group of conditions known as lysosomal storage disorders. In this...

Retinal vein occlusion (RVO) is a serious eye condition that occurs when a vein in the retina becomes blocked. This blockage can lead to...

Ludwig's angina is a serious bacterial infection that affects the floor of the mouth and the neck. It often starts from a tooth infection...

Myotonic dystrophy is a genetic disorder that affects muscles and other parts of the body. This condition can cause muscle weakness,...

Patau Syndrome, also known as Trisomy 13, is a serious genetic disorder caused by the presence of an extra copy of chromosome 13. This...

Hageman Factor Deficiency is a rare blood disorder that affects how blood clots. Although it doesn't usually cause noticeable symptoms,...

A psoas abscess is a serious medical condition characterized by a collection of pus in the psoas muscle, located in the lower back....

Twin-to-Twin Transfusion Syndrome (TTTS) is a serious condition that can happen during pregnancies with identical twins sharing a single...

Meckel's diverticulum is a small pouch that forms in the lower part of the small intestine. It is a common condition that people are...