Symptoms of CYP24A1 Gene Hypercalcemia Infantile Type Genetic Test
Understanding the intricacies of genetic conditions is essential for early diagnosis and treatment. One such condition, hypercalcemia infantile type, linked to mutations in the CYP24A1 gene, has garnered attention for its significant impact on calcium homeostasis in the body. DNA Labs UAE offers a comprehensive genetic test for this condition, priced at 4400 AED, aimed at providing crucial insights for affected families.
Hypercalcemia, characterized by elevated calcium levels in the blood, can manifest in various ways depending on age, severity, and individual health. Infants and young children with mutations in the CYP24A1 gene may exhibit a range of symptoms, which are crucial for parents and healthcare providers to recognize early.
Key Symptoms of Hypercalcemia Infantile Type
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Persistent Vomiting: Infants may experience recurrent vomiting that is not related to infections or other common causes of vomiting in infancy.
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Failure to Thrive: Affected children might show inadequate weight gain and growth compared to their peers, a condition often referred to as failure to thrive.
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Dehydration: Despite adequate fluid intake, infants with this condition can become dehydrated due to the diuretic effect of high calcium levels.
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Urinary Symptoms: Increased calcium can lead to the development of kidney stones, causing pain, discomfort, and potential urinary tract infections.
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Nephrocalcinosis: This condition, characterized by calcification in the kidneys, can lead to impaired kidney function and, in severe cases, kidney failure.
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Neurodevelopmental Delay: High calcium levels can affect the nervous system, potentially leading to delays in reaching developmental milestones.
Early detection and intervention are crucial in managing the symptoms and preventing long-term complications associated with hypercalcemia infantile type. The genetic test offered by DNA Labs UAE for the CYP24A1 gene provides families with the opportunity to understand their risk and seek appropriate treatment and management strategies.
The cost of the test, 4400 AED, reflects the comprehensive analysis and personalized report provided, offering invaluable insights into managing this condition. For more information or to schedule a test, visit DNA Labs UAE.
Understanding the genetic underpinnings of conditions like hypercalcemia infantile type can empower families and healthcare providers to make informed decisions about care and management. Through advanced genetic testing, DNA Labs UAE is committed to providing the tools necessary for early diagnosis and intervention, paving the way for a healthier future for affected children.
