Ewing sarcoma
Ewing sarcoma is a rare genetic disease that affects children and young adults. It is one of the rarest forms of bone cancer, accounting for less than 1% of all childhood cancers. Ewing sarcoma is caused by a specific gene…
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17q12 deletion syndrome
17q12 deletion syndrome, also known as renal cysts and diabetes syndrome (RCAD), is a rare genetic condition caused by a deletion of a small piece of chromosome 17 at position q12. The syndrome is associated with a range of clinical…
Spinosad Topical
Spinosad Topical Spinosad suspension is used to treat head lice (small insects that attach themselves to the scalp) in adults and children 6 months of age and older. It is also used to treat scabies (mites that attach themselves to…
CTNND1 gene
The CTNND1 gene is an important gene that is related to various diseases and conditions. It has been extensively studied and researched in the field of genetics and health. Many scientific articles and research papers have been published on this…
Opioid Testing
Opioid testing refers to the process of conducting screenings and investigation to determine if a person has used opioids. These tests are often ordered by healthcare providers to help give them a better understanding of the amount of opioids in…
OBSL1 gene
The OBSL1 gene, also known as obscurin-like 1, is a genetic precursor gene that codes for obscurin-like proteins. These proteins play an important role in various biological processes and are associated with multiple health conditions, including genetic disorders and syndromes.…
HSD3B2 gene
The HSD3B2 gene, also known as 3β-Hydroxysteroid dehydrogenase/Delta 5-Delta 4-isomerase, plays a crucial role in the genetic regulation of aldosterone, the salt-retaining hormone. This gene is associated with a novel variant of 3β-HSD deficiency, which is characterized by changes in…
What are single nucleotide polymorphisms SNPs
Single nucleotide polymorphisms (SNPs) are the most common type of genetic variation that occur within the human genome. SNPs are tiny changes in a single nucleotide base pair, and they can have a significant impact on an individual’s susceptibility to…
HRAS gene
The HRAS gene is a gene that plays a crucial role in the development and growth of cells in the body. It is part of a family of oncogenes, which are genes that have the potential to cause cancer. Mutations…
EIF2B4 gene
The EIF2B4 gene, also known as eukaryotic translation initiation factor 2B subunit delta (EIF2Bδ), is a gene that plays a crucial role in protein synthesis. It is responsible for producing a protein called eukaryotic translation initiation factor 2B, which regulates…