Expert

The MT-ND1 gene is part of a complex system of genes that are responsible for the production of resources and energy within our bodies. It is one of the genes that is commonly tested for in genetic testing. The MT-ND1…

Wagner syndrome is a rare genetic condition that affects vision. It is caused by mutations in the genes associated with vitreoretinopathy, a disorder that affects the back of the eye. The syndrome is named after the German ophthalmologist, Dr. U.…

The POLR3B gene, also known as polymerase (RNA) III (DNA directed) polypeptide B, is responsible for encoding one of the subunits of RNA polymerase III, an enzyme involved in RNA synthesis. This gene is related to POLR3-related leukodystrophy, a genetic…

Clopidogrel resistance is a condition where patients do not respond to the benefits of clopidogrel, a medication that helps prevent blood clots from forming in the body. This resistance can be caused by genetic factors, specifically genes like CYP2C19 and…

Intestinal pseudo-obstruction is a rare condition that has been the subject of scientific research by certain experts in the field. According to a study by Wangler et al., this condition is associated with a variety of genetic causes and can…

Arterial tortuosity syndrome is a rare genetic disorder that is characterized by abnormalities in the arteries and other tissues of the body. This condition is associated with the abnormal growth and development of the arterial system, causing the arteries to…

The PIGT gene is a certain gene that plays a crucial role in the body’s production of proteins. It is involved in a process called pig-t, which is responsible for the synthesis of certain proteins that are important for the…

Alzheimer’s disease (AD), the most common cause of dementia in older people, is a neurodegenerative condition that affects the brain and leads to a gradual decline in cognitive function, memory loss, and changes in behavior. The exact cause of Alzheimer’s…

Subcortical band heterotopia, also known as double cortex syndrome, is a rare genetic disorder characterized by the presence of an additional band of neurons located below the normal cortex. This condition is caused by mutations in certain genes associated with…

Congenital mirror movement disorder, also known as “mirror movements,” is a rare genetic condition in which an individual experiences involuntary movements on one side of the body that mirror intentional movements on the opposite side. These movements typically develop in…