Symptoms and Testing information for ROBO2 Gene Vesicoureteral reflux type 2 Genetic Test

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

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

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 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 […]

Symptoms and Testing information for WNT4 Gene SERKAL syndrome Genetic Test

Symptoms and Testing information for WNT4 Gene SERKAL syndrome Genetic Test

In the realm of medical genetics, the exploration of specific gene mutations and their associated syndromes has opened new avenues for diagnosis and treatment. One such breakthrough has been in the understanding of the WNT4 gene and its link to SERKAL syndrome. DNA Labs UAE stands at the forefront of this research, offering a comprehensive […]

Symptoms and Testing information for LAS1L Gene Wilson-Turner syndrome Genetic Test

Symptoms and Testing information for LAS1L Gene Wilson-Turner syndrome Genetic Test

Symptoms of LAS1L Gene Wilson-Turner Syndrome Genetic Test Wilson-Turner Syndrome is a rare genetic disorder that primarily affects males, characterized by intellectual disability, obesity, gynecomastia (enlarged breasts in males), and distinct facial features. It is caused by mutations in the LAS1L gene located on the X chromosome. Understanding the symptoms and undergoing genetic testing can […]

Symptoms and Testing information for RBM8A Gene Thromocytopenia-Absent-Radius-Syndrome Genetic Test

Symptoms and Testing information for RBM8A Gene Thromocytopenia-Absent-Radius-Syndrome Genetic Test

Understanding the complexities of genetic conditions is essential for effective diagnosis and treatment. One such rare but significant condition is Thrombocytopenia-Absent-Radius (TAR) Syndrome, linked to mutations in the RBM8A gene. DNA Labs UAE is at the forefront of genetic testing, offering comprehensive evaluations for individuals suspected of having this condition. The RBM8A Gene Thrombocytopenia-Absent-Radius-Syndrome Genetic […]

Symptoms and Testing information for EIF2AK3 Gene Wolcott-Rallison syndrome Genetic Test

Symptoms and Testing information for EIF2AK3 Gene Wolcott-Rallison syndrome Genetic Test

Wolcott-Rallison Syndrome (WRS) is a rare genetic disorder primarily characterized by the onset of early infancy diabetes, multiple epiphyseal dysplasia, and a range of other possible systemic manifestations. The disorder is attributed to mutations in the EIF2AK3 gene, which plays a critical role in protein synthesis and the stress response of the endoplasmic reticulum. Due […]

Symptoms and Testing information for SLC5A5 Gene Thyroid dyshormonogenesis type 1 Genetic Test

Symptoms and Testing information for SLC5A5 Gene Thyroid dyshormonogenesis type 1 Genetic Test

Understanding the nuances of our genetic makeup has become a cornerstone of modern medicine, enabling us to predict, diagnose, and treat various genetic disorders with unprecedented precision. One such condition that has garnered attention is thyroid dyshormonogenesis type 1, a disorder stemming from mutations in the SLC5A5 gene. DNA Labs UAE stands at the forefront […]

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