Symptoms and Testing information for GNA13 Gene Vascular System Defects Due to GNA13 Deficiency Genetic Test

Symptoms and Testing information for GNA13 Gene Vascular System Defects Due to GNA13 Deficiency Genetic Test

The vascular system plays a critical role in maintaining the homeostasis of the human body, distributing essential nutrients and oxygen to various organs while removing waste products. Genetic abnormalities can significantly impair this system’s functionality, leading to severe health implications. One such genetic concern is related to the GNA13 gene, which, when deficient, can lead […]

Symptoms and Testing information for RASA1 Gene Parkes Weber Syndrome Genetic Test

Symptoms and Testing information for RASA1 Gene Parkes Weber Syndrome Genetic Test

Symptoms of RASA1 Gene Parkes Weber Syndrome Genetic Test Parkes Weber Syndrome is a rare congenital condition characterized by a combination of arteriovenous malformations (AVMs) and capillary malformation-arteriovenous malformations (CM-AVMs). These vascular anomalies can lead to a range of symptoms, varying in severity among individuals. The RASA1 gene plays a crucial role in the development […]

Symptoms and Testing information for ADA2 Gene Polyarteritis Nodosa Childhood-Onset Genetic Test

Symptoms and Testing information for ADA2 Gene Polyarteritis Nodosa Childhood-Onset Genetic Test

Polyarteritis nodosa (PAN) is a rare, potentially life-threatening disease characterized by the inflammation of blood vessels (vasculitis), which can damage organs throughout the body. The childhood-onset form of this disease, associated with mutations in the ADA2 gene, presents unique challenges and symptoms that are critical to recognize for early diagnosis and treatment. DNA Labs UAE […]

Symptoms and Testing information for PROC Gene Protein C Deficiency AD Genetic Test

Symptoms and Testing information for PROC Gene Protein C Deficiency AD Genetic Test

### Article: Protein C deficiency is a rare genetic disorder that affects the blood’s ability to clot properly, leading to an increased risk of developing blood clots. The PROC gene is responsible for producing protein C, and mutations in this gene can lead to either Type I or Type II protein C deficiency. Understanding the […]

Symptoms and Testing information for KLHL3 Gene Pseudohypoaldosteronism Type 2D Genetic Test

Symptoms and Testing information for KLHL3 Gene Pseudohypoaldosteronism Type 2D Genetic Test

Pseudohypoaldosteronism Type 2D, also known as Familial Hyperkalemia and Hypertension (FHHt), is a rare genetic disorder that disrupts the normal balance of potassium, sodium, and chloride in the body. This imbalance leads to a range of symptoms and complications. The KLHL3 gene has been identified as one of the genetic contributors to this condition. DNA […]

Symptoms and Testing information for NR3C2 Gene Hypertension Early Onset Genetic Test

Symptoms and Testing information for NR3C2 Gene Hypertension Early Onset Genetic Test

In the realm of medical genetics, understanding the underlying causes of diseases has always been a cornerstone for developing effective treatments and preventive measures. One such condition that has garnered significant attention is hypertension, particularly the early-onset form that is influenced by genetic factors. Among the genes implicated in this condition, the NR3C2 gene plays […]

Symptoms and Testing information for CUL3 Gene Pseudohypoaldosteronism Type 2E Genetic Test

Symptoms and Testing information for CUL3 Gene Pseudohypoaldosteronism Type 2E Genetic Test

Pseudohypoaldosteronism Type 2E, also known as Familial Hyperkalemia and Hypertension (FHHt), is a rare genetic disorder that affects the body’s ability to properly regulate blood pressure and potassium levels. It is caused by mutations in the CUL3 gene, which plays a crucial role in the regulation of electrolyte balance and blood pressure. Recognizing the symptoms […]

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