Diarrhea type 3 secretory sodium congenital syndromic, often referred to as congenital sodium diarrhea (CSD), is a rare genetic disorder that affects the body’s ability to properly absorb sodium through the intestines. This condition is caused by mutations in the SPINT2 gene, which plays a crucial role in the regulation of sodium channels in the […]
Fanconi anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. The FANCD2 gene plays a critical role in the FA pathway, a cellular defense system against DNA damage. Mutations in the FANCD2 gene can cause Fanconi anemia type D2, one of the more severe forms of the disease. Recognizing the […]
The NEUROG3 gene plays a pivotal role in the development of the endocrine pancreas and is crucial for the differentiation of enteroendocrine cells in the gastrointestinal tract. Mutations in the NEUROG3 gene can lead to a rare but severe disorder known as congenital malabsorptive diarrhea type 4. This condition is characterized by a range of […]
Fanconi anemia is a rare genetic disorder that affects the bone marrow, leading to decreased production of all types of blood cells. Among the various types of Fanconi anemia, type E, caused by mutations in the FANCE gene, is one of the less common subtypes. Recognizing the symptoms associated with this condition is crucial for […]
In the realm of personalized medicine, genetic testing plays a pivotal role in understanding an individual’s susceptibility to various conditions and their response to certain medications. One such critical genetic test is for DPYD gene dihydropyrimidine dehydrogenase deficiency. This deficiency can significantly impact the body’s ability to metabolize certain chemotherapy drugs, leading to severe and […]
Symptoms of FANCF Gene Fanconi Anemia Type F Genetic Test Fanconi Anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. It is caused by genetic mutations in one of several genes, with the FANCF gene being one such example. This condition is characterized by physical abnormalities, bone marrow failure, and […]
Dihydropyrimidinuria is a rare genetic disorder that affects the body’s ability to break down certain components of proteins, specifically the pyrimidine bases of uracil and thymine. This condition is caused by mutations in the DPYS gene, which is crucial for the normal function of the enzyme dihydropyrimidine dehydrogenase (DPD). DPD plays a vital role in […]
Fanconi anemia (FA) is a rare, inherited blood disorder that leads to bone marrow failure. It is caused by genetic mutations in one of at least 22 genes, with the FANCG gene being one of them. This condition is characterized by physical abnormalities, bone marrow failure, and an increased risk of cancer. Early diagnosis through […]
Symptoms of DMGDH Gene Dimethylglycine Dehydrogenase Deficiency Dimethylglycine Dehydrogenase (DMGDH) deficiency is a rare genetic disorder that affects the body’s ability to metabolize certain amino acids properly. This condition can lead to a variety of health issues, ranging from mild to severe. Recognizing the symptoms early can be crucial for managing the condition effectively. Some […]
Diabetes mellitus type 1, also known as type 1 diabetes, is a form of diabetes mellitus that results from the autoimmune destruction of the insulin-producing beta cells in the pancreas. The subsequent lack of insulin leads to increased blood and urine glucose. The classical symptoms are frequent urination, increased thirst, increased hunger, and weight loss. […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
