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PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test

Original price was: $700.Current price is: $500.

-29%

The PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test is a comprehensive genetic analysis that identifies mutations in the PREPL gene responsible for a rare autosomal recessive disorder. This advanced next-generation sequencing test detects genetic variations causing hypotonia (muscle weakness), cystinuria (kidney stone formation), and growth hormone deficiency. The test provides crucial diagnostic information for patients presenting with unexplained muscle weakness, recurrent kidney stones, and developmental delays. At only $500 USD, this specialized genetic testing offers definitive diagnosis, enabling targeted treatment strategies and genetic counseling for affected families. Results are typically available within 3-4 weeks using blood, extracted DNA, or FTA card samples.

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PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test

Comprehensive Genetic Analysis for Rare Metabolic Disorders

The PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test represents a cutting-edge diagnostic tool for identifying mutations in the PREPL (Prolyl Endopeptidase-Like) gene, which is responsible for a rare autosomal recessive disorder affecting multiple body systems. This sophisticated genetic test utilizes next-generation sequencing technology to provide comprehensive analysis of the PREPL gene, enabling accurate diagnosis and personalized treatment planning for patients with complex neuromuscular and metabolic symptoms.

What Does This Test Measure and Detect?

This advanced genetic test specifically targets and analyzes the PREPL gene to identify pathogenic variants, including:

  • Point mutations, insertions, and deletions in the PREPL gene
  • Autosomal recessive inheritance patterns
  • Genetic markers associated with hypotonia-cystinuria syndrome
  • Variants affecting prolyl endopeptidase enzyme function
  • Mutations impacting neurotransmitter metabolism and amino acid transport

Who Should Consider This Genetic Test?

This specialized genetic testing is recommended for individuals presenting with the following symptoms or clinical indications:

  • Unexplained muscle weakness (hypotonia) in infancy or childhood
  • Recurrent kidney stones or cystinuria diagnosis
  • Growth hormone deficiency or growth retardation
  • Developmental delays and feeding difficulties
  • Family history of PREPL gene disorders
  • Consanguineous parentage with similar symptoms
  • Unexplained metabolic disorders affecting multiple systems
  • Suspected neuromuscular disorders with renal complications

Clinical Benefits of PREPL Gene Testing

Undergoing this comprehensive genetic analysis provides numerous clinical advantages:

  • Definitive Diagnosis: Confirms or rules out PREPL gene mutations as the underlying cause of symptoms
  • Personalized Treatment: Enables targeted therapeutic interventions based on genetic findings
  • Family Planning: Provides crucial information for genetic counseling and reproductive decisions
  • Early Intervention: Facilitates timely management of neuromuscular and metabolic complications
  • Prognostic Information: Helps predict disease progression and potential complications
  • Reduced Diagnostic Odyssey: Minimizes unnecessary testing and medical procedures

Understanding Your Test Results

Your genetic test results will be carefully interpreted by our expert geneticists and provide clear guidance:

  • Positive Result: Indicates the presence of pathogenic PREPL gene mutations, confirming the diagnosis of hypotonia-cystinuria syndrome
  • Negative Result: Suggests that PREPL gene mutations are not the cause of your symptoms, directing further diagnostic evaluation
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact, requiring additional family studies
  • Carrier Status: Determines if you carry one copy of a mutated PREPL gene without showing symptoms

All results include comprehensive genetic counseling to ensure proper understanding and appropriate next steps for medical management.

Test Pricing and Availability

Test Component Price (USD)
PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test – Discount Price $500
PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test – Regular Price $700

Nationwide Testing Availability

General Genetics Corporation provides comprehensive genetic testing services across the United States, with convenient testing locations in all major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our nationwide network ensures accessible genetic testing for patients throughout the country.

Sample Collection and Processing

This test requires one of the following sample types:

  • Blood sample (standard venipuncture)
  • Extracted DNA sample
  • One drop of blood on FTA card

Turnaround Time: 3 to 4 weeks
Pre-test Requirements: Clinical history documentation and genetic counseling session to create a family pedigree chart

Take Control of Your Genetic Health Today

Don’t let uncertainty about your genetic health prevent you from getting the answers you need. Our PREPL Gene Hypotonia-Cystinuria Syndrome NGS Genetic DNA Test provides the comprehensive genetic analysis required for accurate diagnosis and effective treatment planning. With our discounted price of $500 USD and nationwide availability, advanced genetic testing has never been more accessible.

Call or WhatsApp us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our genetic specialists are ready to help you understand your genetic health and provide the clarity you deserve.