Enzymes’ function is to help trigger bodily processes ranging from digestion to blood clotting to growth. There are many ...

According to CDC, sickle cell is a genetic condition present at birth, inherited when a child receives two genes—one from ...

Data presentations highlight the results for FILSPARI® (sparsentan), the only approved kidney-targeted medicine for IgA nephropathy, when used as a first-line treatment, and in combination with other ...

By the time Noah Jordan was diagnosed with a rare mitochondrial disease, his parents were told there was no cure ...

In today's show we will cover Alagille Syndrome.Alagille syndrome is a rare genetic disorder caused by mutations in the JAG1 ...

The types are also sometimes described as shortages of particular proteins needed for normal liver function. Each type has a different genetic cause. In addition to signs and symptoms related to liver ...

For a person with allergies, the body’s immune system reacts and produces immunoglobulin type E antibodies, or IgE, in response to the allergen. Research conducted on allergies has shown a genetic ...

Hundreds of babies have begun to be tested for over 200 rare genetic conditions as part of a world-leading study in NHS hospitals that aims to screen up to 100,000 newborns in England. The pioneering ...

Hundreds of babies have begun to be tested for over 200 rare genetic conditions as part of a world-leading study in NHS hospitals that aims to screen up to 100,000 newborns in England. The Generation ...

A team of international scientists has uncovered the genetic underpinnings of a rare, inherited autoimmune disorder, according to a study recently published in Science Translational Medicine.

Elevations in serum bilirubin during treatment with lapatinib ... from patients participating in clinical trials enables genetic characterization of drug-induced liver injury events, identified ...