Expert

Expert

Melanoma

Melanoma is a rare and potentially deadly skin condition that is often associated with genetic factors. According to the American Academy of Dermatology, melanoma is the most dangerous form of skin cancer, with over 100,000 new cases diagnosed each year…

CHD7 gene

The CHD7 gene is associated with a variety of syndromes and disorders, including CHARGE syndrome, a rare genetic disorder characterized by a wide range of birth defects. CHD7 stands for “chromodomain helicase DNA binding protein 7”. CHD7 gene mutations can…

ATP1A1 gene

The ATP1A1 gene, also known as the alpha-a subunit of the Na+/K+ -ATPase, is a genetic variant that has been associated with several diseases and conditions. One of these conditions is Charcot-Marie-Tooth disease, a neurological disorder that affects the peripheral…

TPMT gene

The TPMT gene is a catalog of health-related information for the TPMT gene. This gene is known for its role in immune response and is considered a genetic variant in pharmacogenetics. The TPMT gene is listed as one of the…

ALT Blood Test

ALT stands for alanine aminotransferase, which is an enzyme found mostly in the liver. The ALT blood test is a common test used to assess liver function and detect liver damage. There are various reasons why someone may need to…

DNAI1 gene

The DNAI1 gene is known to be associated with various conditions, including primary ciliary dyskinesia (PCD), heterotaxy syndrome, and other ciliary diseases. It codes for a protein that plays a crucial role in the function of cilia, which are important…

Mevalonate kinase deficiency

Mevalonate kinase deficiency, also known as mevalonic aciduria or hyper-immunoglobulinemia D syndrome (HIDS), is a rare genetic condition that affects the activity of the mevalonate kinase gene. This condition is characterized by recurrent episodes of fever, skin rash, diarrhea, and…

Certolizumab Injection

Certolizumab Injection Certolizumab injection may decrease your ability to fight infection and increase the risk that you will get a serious or life-threatening infection including severe fungal, bacterial, and viral infections that may spread through the body. These infections may…

Fosphenytoin Injection

Fosphenytoin Injection You may experience serious or life-threatening low blood pressure or irregular heart rhythms while you are receiving fosphenytoin injection or afterwards. Tell your doctor if you have or have ever had irregular heart rhythms or heart block (condition…

Complete LCAT deficiency

Complete LCAT deficiency Complete LCAT deficiency, also known as familial lecithin-cholesterol acyltransferase (LCAT) deficiency, is a genetic condition that affects the functions of the LCAT gene. This rare genetic disorder can lead to various health problems and complications. Complete LCAT…