Symptoms and Testing information for CACNB4 Gene Episodic ataxia type 5 Genetic Test

Symptoms and Testing information for CACNB4 Gene Episodic ataxia type 5 Genetic Test

Episodic ataxia type 5 is a rare genetic disorder that affects the nervous system, leading to intermittent episodes of poor coordination and balance (ataxia). This condition is caused by mutations in the CACNB4 gene, which plays a crucial role in the proper functioning of calcium channels in the body. These channels are essential for the normal transmission of signals in the nervous system. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for episodic ataxia type 5, aimed at identifying mutations in the CACNB4 gene.

Symptoms of Episodic Ataxia Type 5

The symptoms of episodic ataxia type 5 can vary widely among affected individuals, but they typically include:

  • Intermittent Ataxia: Episodes of uncoordinated movements that can affect gait, balance, and manual dexterity. These episodes can last from minutes to hours and may occur unpredictably.
  • Vertigo and Dizziness: Many individuals experience episodes of vertigo or dizziness, which may or may not accompany the ataxia.
  • Muscle Weakness: Episodes may also include muscle weakness, further complicating movement and coordination.
  • Headaches: Migraine-like headaches can occur, often preceding or accompanying the ataxic episodes.
  • Seizures: In some cases, individuals with episodic ataxia type 5 may experience seizures, although this is less common.

It’s important to note that the frequency and severity of these symptoms can vary, and not all individuals will experience all symptoms. Early diagnosis and management are key to improving quality of life for those affected.

Genetic Test for Episodic Ataxia Type 5

DNA Labs UAE provides a genetic test specifically designed to identify mutations in the CACNB4 gene associated with episodic ataxia type 5. This test is a crucial step in the diagnosis of the condition, enabling healthcare providers to offer targeted management strategies for affected individuals.

The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the CACNB4 gene. The results of this test can help confirm a diagnosis of episodic ataxia type 5 and guide treatment and management decisions.

The cost of the genetic test for episodic ataxia type 5 at DNA Labs UAE is 4400 AED. This investment includes the cost of the sample collection, genetic analysis, and a comprehensive report of the findings. For more information and to schedule a test, please visit DNA Labs UAE.


Episodic ataxia type 5 is a challenging condition, but early diagnosis and targeted management can significantly improve the quality of life for those affected. Understanding the symptoms is the first step toward recognizing the need for further evaluation. The genetic test offered by DNA Labs UAE for mutations in the CACNB4 gene is a critical tool in the diagnosis and management of this condition. If you or someone you know is experiencing symptoms consistent with episodic ataxia type 5, consider reaching out to DNA Labs UAE for more information on genetic testing.

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