Thyroid dyshormonogenesis is a condition that affects the thyroid gland, impairing its ability to produce hormones properly. Among the various types of thyroid dyshormonogenesis, Type 6 is particularly notable for its genetic basis, linked to mutations in the DUOX1 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs […]
Nephrology Diseases
Symptoms and Testing information for DUOX2 Gene Thyroid dyshormonogenesis type 6 Genetic Test
DNA Labs UAE is at the forefront of genetic testing, providing a comprehensive range of services designed to offer insights into various health conditions, including thyroid disorders. Among these, the DUOX2 Gene Thyroid Dyshormonogenesis Type 6 Genetic Test stands out as a crucial tool for diagnosing a specific type of congenital hypothyroidism, a condition that […]
Symptoms and Testing information for SECISBP2 Gene Thyroid hormone metabolism abnormal Genetic Test
Understanding the SECISBP2 Gene and Its Role in Thyroid Hormone Metabolism The SECISBP2 gene, also known as SBP2, plays a pivotal role in the human body’s thyroid hormone metabolism. Thyroid hormones are crucial for regulating metabolism, heart and digestive functions, muscle control, brain development, and maintenance of bones. Abnormalities in the SECISBP2 gene can lead […]
Symptoms and Testing information for THRB Gene Thyroid hormone resistance Genetic Test
Symptoms of THRB Gene Thyroid Hormone Resistance Genetic Test The THRB gene plays a pivotal role in the body’s thyroid hormone pathway, influencing numerous physiological processes. Mutations in the THRB gene can lead to thyroid hormone resistance, a condition where the body’s cells are insensitive to the thyroid hormone. This can disrupt normal metabolic functions, […]
Symptoms and Testing information for HADHB Gene Trifunctional protein deficiency Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, providing comprehensive solutions for a wide array of genetic conditions. Among the tests offered is the HADHB Gene Trifunctional Protein Deficiency Genetic Test, a crucial examination for individuals suspected of having this rare genetic disorder. This article aims to shed light on the […]
Symptoms and Testing information for CRB2 Gene Ventriculomegaly with cystic kidney disease Genetic Test
At DNA Labs UAE, we are dedicated to providing our clients with comprehensive genetic testing services that help in diagnosing and understanding various genetic disorders. One such condition that has come under increased scrutiny is the syndrome associated with mutations in the CRB2 gene, which can lead to ventriculomegaly and cystic kidney disease. This condition […]
Symptoms and Testing information for ROBO2 Gene Vesicoureteral reflux type 2 Genetic Test
Vesicoureteral reflux (VUR) is a condition where urine flows backward from the bladder to the kidneys. This reverse flow can lead to kidney infections and damage. There are various types of VUR, and one of the genetic forms is associated with mutations in the ROBO2 gene, known as Vesicoureteral reflux type 2. Understanding the symptoms […]
Symptoms and Testing information for SOX17 Gene Vesicoureteral reflux type 3 Genetic Test
Vesicoureteral reflux (VUR) is a condition where urine flows backward from the bladder to the kidneys. This reverse flow can lead to various complications, including urinary tract infections and kidney damage. VUR is categorized into different types, with Type 3 being one of the classifications. Recent studies have identified a genetic link to VUR, specifically […]
Symptoms and Testing information for WDR19 Gene Senior-Loken syndrome type 8 Genetic Test
Understanding the complexities of genetic conditions is crucial for early diagnosis and management. Among these, the WDR19 gene-related Senior-Loken syndrome type 8 is a condition that demands attention due to its significant impact on individuals’ health. DNA Labs UAE is at the forefront of providing comprehensive genetic testing services, including tests for this particular syndrome. […]
Symptoms and Testing information for WT1 Gene Wilms tumor type 1 familial Genetic Test
Symptoms of WT1 Gene Wilms Tumor Type 1 Familial Genetic Test Price 4400 AED Wilms tumor, also known as nephroblastoma, is a rare kidney cancer that primarily affects children. It is associated with mutations in the WT1 gene, which plays a crucial role in kidney development. Recognizing the symptoms early can lead to timely diagnosis […]