FRASER SYNDROME GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited    
The Fraser Syndrome Gene Panel by NGS is a specialized genetic test used to detect mutations in genes such as FRAS1, FREM2, and GRIP1, which are associated with Fraser syndrome. This rare congenital disorder is characterized by cryptophthalmos, syndactyly, renal abnormalities, and developmental issues. Using an EDTA blood sample, the test is performed with advanced Next Generation Sequencing for accurate identification of disease-causing variants. Metropolis Healthcare ensures high-quality genetic analysis to support early diagnosis, prenatal counseling, and informed clinical management

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 21,000.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0114

Frequently Asked Questions (FAQ's):

What is Fraser syndrome?
Fraser syndrome is a rare genetic condition marked by eye abnormalities, fused fingers or toes, and possible kidney malformations.

Which genes are tested in this panel?
The panel analyzes FRAS1, FREM2, GRIP1, and other related genes known to cause Fraser syndrome.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses advanced NGS technology to provide precise detection of clinically relevant genetic mutations.

What sample type is needed for this test?
An EDTA whole blood sample is required.

Who should consider this test?
Parents with a previous affected child, individuals with congenital anomalies resembling Fraser syndrome, or families with a known mutation may benefit.

Is any preparation required?
No fasting or special preparation is required prior to sample collection.

How long do results take at Metropolis Healthcare?
Results are typically available within a few working days, depending on laboratory workflow.

How do the results help?
They confirm diagnosis, aid in clinical planning, and provide essential insights for genetic and prenatal counseling

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