Epinephrine Oral Inhalation Epinephrine oral inhalation is used to relieve symptoms of asthma that occur from time to time, including wheezing, chest tightness, and shortness of breath in adults and children 12 years of age and older. Epinephrine oral inhalation…
Factor VII deficiency, also known as congenital factor VII deficiency or hemostasis Wulff syndrome, is a rare genetic disorder that affects the ability of blood to clot. This condition is caused by mutations in the F7 gene, which provides instructions…
Nemaline myopathy is a rare genetic condition that affects the muscles. It is caused by mutations in several genes, including ACTA1, NEB, TPM3, and others. These mutations disrupt the normal contraction of muscle fibers, leading to muscle weakness and other…
Alcohol has become a significant problem in our society, affecting people of all ages and backgrounds. Many individuals struggle with alcohol addiction, experiencing negative consequences in their personal and professional lives. Recognizing and addressing alcohol use problems is crucial for…
The ARSB gene, also known as the N-acetylgalactosamine-4-sulfatase gene, is involved in the production of an enzyme called arylsulfatase B. This gene is responsible for the synthesis of sulfatases, which play a crucial role in the breakdown and recycling of…
The human genome is a complex structure composed of 23 pairs of chromosomes, each containing thousands of genes. Chromosome 14 is one of these pairs and it plays a crucial role in our health and development. It has been linked…
The Zika virus is a mosquito-borne virus that has caused outbreaks in several countries around the world. It is most commonly transmitted through the bite of an infected Aedes mosquito, but it can also be transmitted through sexual contact and…
The Basic Metabolic Panel (BMP) is a group of blood tests that provide important information about the body’s protein and electrolyte levels, as well as its kidney and liver function. These tests can help identify and monitor various conditions and…
2q37 deletion syndrome, also known as “2q37 monosomy” or “deletion 2q37 syndrome”, is a rare genetic condition that occurs when a small piece of genetic material is missing from one of the body’s 46 chromosomes. The condition is caused by…
The roof of the mouth is a vulnerable area in the oral cavity that can develop various types of bumps and growths. These bumps can appear in different sizes, shapes, and colors. They can be uncomfortable and may cause pain…