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CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test

Original price was: KSh 56,000.Current price is: KSh 40,000.

-29%

The CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test is essential for diagnosing metabolic disorders in infants. Priced at 40,000 KSh, this test utilizes NGS technology to detect genetic mutations associated with CPT2 deficiency, providing vital information for early intervention.

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  • 100% Accurate Test Results
  • Get Tested at Nigeria No1 Genetic DNA Lab
  • Customer support Call 0711564616
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CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test
CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test
KSh 56,000 Original price was: KSh 56,000.KSh 40,000Current price is: KSh 40,000.

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CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test

Introduction

The CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test is a crucial diagnostic tool for identifying metabolic disorders in infants. This test uses Next Generation Sequencing (NGS) technology to analyze genetic mutations associated with Carnitine Palmitoyltransferase 2 (CPT2) deficiency, a condition that can lead to serious health complications if not identified early.

What the Test Measures

This genetic test specifically measures mutations in the CPT2 gene, which is essential for the metabolism of fatty acids. By detecting these mutations, healthcare providers can assess the risk of CPT2 deficiency in infants and guide appropriate treatment options.

Who Should Consider This Test?

Parents should consider this test for their infants if there is a family history of metabolic disorders, particularly CPT2 deficiency. Symptoms may include:

  • Severe muscle weakness
  • Hypoglycemia
  • Cardiomyopathy
  • Fatigue or lethargy

Early testing is vital for timely intervention and management of the condition.

Benefits of Taking the Test

  • Early diagnosis of CPT2 deficiency can prevent severe health complications.
  • Guides treatment options and dietary recommendations for affected infants.
  • Provides peace of mind for families with a history of metabolic disorders.

Understanding Your Results

Results from the CPT2 Gene test typically take 3 to 4 weeks. A genetic counseling session is recommended to interpret the results accurately and to discuss potential implications for family members.

Test Pricing

Test Name Discount Price Regular Price
CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test 40000 KSh 56000 KSh

Book Your Test Today!

We have branches across Kenya, including Nairobi, Mombasa, and Kisumu, and offer home sample collection services for your convenience. Don’t wait to ensure your child’s health—book the CPT2 Gene Carnitine Palmitoyltransferase 2 Deficiency Infantile NGS Genetic DNA Test today! Call or WhatsApp us at +254711564616.