PHKA1 gene
The PHKA1 gene, also known as phosphorylase kinase alpha 1, is responsible for the production of subunits of phosphorylase kinase in the liver and muscles. This gene plays a crucial role in the breakdown of glycogen, a stored form of…
The PHKA1 gene, also known as phosphorylase kinase alpha 1, is responsible for the production of subunits of phosphorylase kinase in the liver and muscles. This gene plays a crucial role in the breakdown of glycogen, a stored form of…
When it comes to drug testing, it is important to understand what the results mean and what they can tell you. Whether you’re using drugs for recreational purposes or are prescribed medication, drug testing can help employers determine if someone…
Mechlorethamine Topical Mechlorethamine gel is used to treat early stage mycosis fungoides-type cutaneous T-cell lymphoma (CTCL; a cancer of the immune system that begins with skin rashes) in people who have received previous skin treatment. Mechlorethamine gel is in a…
Diastrophic dysplasia is a rare genetic condition characterized by skeletal abnormalities and short stature. It is one of the more common types of dwarfism, with an estimated frequency of 1 in 100,000 newborns. This condition is associated with mutations in…
Succinate-CoA ligase deficiency, also known as suclg1 deficiency, is a rare genetic condition associated with the depletion of succinate-CoA ligase, an enzyme crucial for the metabolism of succinate-coenzyme A (succinyl-CoA). This condition is caused by mutations in the SUCGL1 gene,…
Toremifene Toremifene may cause QT prolongation (an irregular heart rhythm that can lead to fainting, loss of consciousness, seizures, or sudden death). Tell your doctor if you or anyone in your family has or has ever had long QT syndrome…
Clindamycin and Benzoyl Peroxide Topical The combination of clindamycin and benzoyl peroxide is used to treat acne. Clindamycin and benzoyl peroxide are in a class of medications called topical antibiotics. The combination of clindamycin and benzoyl peroxide works by killing…
The PMS2 gene is a crucial component of the DNA mismatch repair (MMR) system. While the MMR system is primarily known for its role in correcting DNA replication errors, it also plays an essential role in maintaining the stability of…
Many people can experience hearing loss as they get older. It is important to be aware of the signs and symptoms of hearing loss, as early detection can lead to better treatment outcomes. Hearing tests, also known as audiometry tests,…
Hereditary Sensory Neuropathy Type IA (HSN IA), also known as Morbus Hereditary Sensory and Autonomic Neuropathy Type IA (HSAN IA), is a rare genetic condition characterized by the progressive degeneration of sensory nerve fibers. HSN IA is caused by mutations…