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LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test

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

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The LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test is a specialized diagnostic tool that identifies mutations in the LAMC1 gene associated with severe brain development abnormalities. This comprehensive next-generation sequencing test provides crucial insights for families affected by Dandy-Walker syndrome, a condition characterized by malformations in the cerebellum and fourth ventricle. The test helps confirm diagnoses, assess recurrence risks, and guide treatment planning. Available for $500 USD, this advanced genetic analysis requires a simple blood sample or extracted DNA and delivers results within 3-4 weeks. Genetic counseling is recommended before testing to ensure proper understanding of results and implications for family planning.

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LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test

Comprehensive Genetic Testing for Brain Development Disorders

The LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying genetic mutations associated with severe congenital brain abnormalities. This specialized test utilizes next-generation sequencing technology to analyze the LAMC1 gene, which plays a critical role in brain development and structural formation during embryonic growth.

What Does This Test Measure and Detect?

This advanced genetic test specifically targets mutations in the LAMC1 gene that are known to cause:

  • Dandy-Walker malformation – a congenital brain abnormality affecting the cerebellum
  • Occipital cephaloceles – neural tube defects where brain tissue protrudes through openings in the skull
  • Associated developmental delays and neurological complications
  • Genetic variants affecting laminin gamma-1 protein function

The test employs sophisticated NGS technology to sequence the entire LAMC1 gene, identifying both known pathogenic variants and novel mutations that may contribute to these complex neurological conditions.

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals presenting with:

  • Prenatal ultrasound findings suggesting Dandy-Walker malformation
  • Newborns with enlarged posterior fossa or cerebellar abnormalities
  • Children with developmental delays and characteristic facial features
  • Family history of neural tube defects or brain malformations
  • Previous pregnancies affected by occipital cephaloceles
  • Unexplained hydrocephalus or increased intracranial pressure
  • Motor coordination difficulties and balance problems

Clinical Benefits of LAMC1 Genetic Testing

Undergoing this comprehensive genetic analysis provides numerous advantages:

  • Accurate Diagnosis: Confirms or rules out genetic causes of brain malformations
  • Family Planning Guidance: Helps assess recurrence risks for future pregnancies
  • Personalized Management: Enables targeted treatment and intervention strategies
  • Early Intervention: Facilitates timely developmental support and therapies
  • Genetic Counseling: Provides families with comprehensive understanding of condition inheritance
  • Research Contribution: Advances scientific knowledge about rare genetic disorders

Understanding Your Test Results

Your genetic test results will be thoroughly explained by our certified genetic counselors:

  • Positive Result: Indicates the presence of a pathogenic LAMC1 mutation, confirming genetic diagnosis
  • Negative Result: Suggests no detectable mutation in LAMC1 gene, though other genetic causes may exist
  • Variant of Uncertain Significance: Identifies genetic changes with unknown clinical impact requiring further evaluation
  • Carrier Status: Determines if individuals carry one copy of mutated gene without showing symptoms

Our genetic counseling team provides comprehensive post-test guidance, helping you understand the implications of your results and connecting you with appropriate medical specialists and support resources.

Test Pricing and Availability

Test Component Price (USD)
Discount Price $500
Regular Price $700
Turnaround Time 3-4 Weeks
Sample Type Blood, Extracted DNA, or Blood on FTA Card

Nationwide Testing Availability

We have conveniently located testing centers across the United States, including major metropolitan areas such as New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, San Jose, and many other cities. Our network of certified genetic counselors and medical professionals ensures you receive consistent, high-quality care regardless of your location.

Pre-Test Preparation and Requirements

Before scheduling your LAMC1 genetic test, we recommend:

  • Comprehensive clinical history documentation
  • Genetic counseling session to discuss testing implications
  • Family pedigree analysis to identify inheritance patterns
  • Review of previous imaging studies and medical records
  • Discussion of potential outcomes and their significance

Our team specializes in pediatric genetics and dysmorphology, providing expert guidance throughout the testing process.

Take the Next Step Toward Genetic Clarity

Don’t let uncertainty about genetic conditions affect your family’s future. Our LAMC1 Gene Dandy-Walker Malformation and Occipital Cephaloceles NGS Genetic DNA Test provides the answers you need to make informed medical decisions. With advanced NGS technology and expert genetic counseling, we deliver comprehensive insights into complex brain development disorders.

Call us today at +1(267) 388-9828 to schedule your genetic counseling session and book your test. Our compassionate team is ready to guide you through every step of the genetic testing process, providing the clarity and support your family deserves.