The MANBA gene is a gene that is responsible for the production of the enzyme beta-mannosidase. This enzyme plays a crucial role in breaking down complex sugars in the body. The information about this gene and its associated health conditions…
The field of genetics has made significant progress in recent years, with the discovery of numerous genes that play crucial roles in various biological processes. One such group of genes, known as Genes X, has attracted considerable attention from scientists…
Genetic testing is a whole range of tests conducted to analyze a person’s DNA, particularly their genome. This form of testing provides valuable information about an individual’s genetic makeup and can be utilized for a variety of purposes, including identifying…
Genetic conditions are disorders that are caused by abnormalities in a person’s genes or chromosomes. One such genetic condition is Seedarier, which is caused by a mutation in the DNajc19 gene. This condition affects the growth and development of the…
Primary ciliary dyskinesia (PCD) is a rare genetic condition associated with abnormalities in the functioning of cilia, which are the hair-like structures that line the respiratory tract and other tissues in the body. These cilia play a crucial role in…
Progressive Familial Intrahepatic Cholestasis (PFIC) is a rare genetic condition that causes the damaging buildup of bile acids and phospholipids in the liver. This buildup results in cholestasis, a condition characterized by impaired bile flow. There are several types of…
The PIGA gene, also known as Phosphatidylinositol Glycan Anchor Biosynthesis Class A, plays a crucial role in the production of a specific protein in the body. This gene is related to various diseases and conditions, including paroxysmal nocturnal hemoglobinuria (PNH)…
Progressive external ophthalmoplegia (PEO) is a rare genetic condition that affects the muscles responsible for eye movement. It is characterized by the progressive weakness of the eye muscles, leading to various eye movement abnormalities. PEO can cause drooping of the…
Waldenström macroglobulinemia (WM), also known as lymphoplasmacytic lymphoma, is a rare type of blood cancer that results in the overproduction and accumulation of abnormal proteins called macroglobulins. This condition is often caused by a genetic mutation in the MYD88 gene,…
Neuroblastoma is a type of cancer that often occurs in young children, usually under the age of 5. It is thought to be caused by a genetic mutation that leads to the rapid development and proliferation of neuroblastoma cells. This…