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Symptoms and Testing information for DPYS Gene Dihydropyrimidinuria Genetic Test

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

Symptoms and Testing information for SPINT2 Gene Diarrhea type 3 secretory sodium congenital syndromic Genetic Test

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

Symptoms and Testing information for GLIS3 Gene Diabetes mellitus neonatal Genetic Test

Symptoms of GLIS3 Gene Diabetes Mellitus Neonatal Genetic Test Diabetes mellitus neonatal, a rare form of diabetes, is primarily caused by genetic mutations, one of which is found in the GLIS3 gene. This condition manifests early in life, often immediately after birth or within the first six months. Recognizing the symptoms early is crucial for

Symptoms and Testing information for ABCC8 Gene Diabetes mellitus transient neonatal type 2 Genetic Test

Diabetes Mellitus Transient Neonatal Type 2 (TNDM2) is a rare form of diabetes that appears in the early days or weeks of a newborn’s life but may resolve or improve within a few months or years, only to potentially reappear later in life. This condition is primarily associated with mutations in the ABCC8 gene, which

Symptoms and Testing information for TRMT5 Gene Combined oxidative phosphorylation deficiency type 26 Genetic Test

DNA Labs UAE is at the forefront of genetic testing and personalized medicine, offering a wide range of services designed to provide patients and healthcare providers with the most accurate and actionable genetic information. Among the various tests offered, the TRMT5 Gene Combined Oxidative Phosphorylation Deficiency Type 26 Genetic Test is a critical diagnostic tool

Symptoms and Testing information for TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test

In the realm of genetic testing and diagnostics, DNA Labs UAE stands at the forefront, offering a wide array of genetic tests tailored to diagnose various genetic disorders. Among these, the TSFM Gene Combined Oxidative Phosphorylation Deficiency Type 3 Genetic Test is particularly significant. This test is designed to detect mutations in the TSFM gene,

Symptoms and Testing information for TUFM Gene Combined oxidative phosphorylation deficiency type 4 Genetic Test

At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic makeup and potential health risks. One of the specialized tests we offer is for the TUFM gene, which is linked to Combined Oxidative Phosphorylation Deficiency Type 4 (COXPD4). This condition is a rare genetic

Symptoms and Testing information for C12ORF65 Gene Combined oxidative phosphorylation deficiency type 7 Genetic Test

Understanding the C12ORF65 Gene and Its Implications Genetic testing has become a cornerstone in the diagnosis and understanding of various inherited disorders. Among these, the C12ORF65 gene plays a critical role in mitochondrial function. Mutations in this gene can lead to Combined Oxidative Phosphorylation Deficiency Type 7, a rare but serious condition that affects multiple

Symptoms and Testing information for ACSF3 Gene Combined malonic and methylmalonic aciduria Genetic Test

Genetic testing has revolutionized the way we understand and approach healthcare, offering insights into inherited diseases and conditions that were previously elusive. Among the various genetic tests available, the ACSF3 Gene Combined Malonic and Methylmalonic Aciduria Genetic Test stands out for its importance in diagnosing a rare but significant metabolic disorder. This test, offered by

Symptoms and Testing information for GFM1 Gene Combined oxidative phosphorylation deficiency type 1 Genetic Test

In the realm of genetic testing, advancements have enabled us to diagnose and understand a plethora of genetic disorders that were once mysteries. Among these, the GFM1 gene mutation, responsible for combined oxidative phosphorylation deficiency type 1, is a condition that has gained attention for its complex presentation and the critical need for early diagnosis.