CARNEY COMPLEX (PRKAR1A) GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited   
The Carney Complex (PRKAR1A) Gene Panel by NGS from Metropolis Healthcare detects mutations in the PRKAR1A gene, which are associated with Carney complex—a rare genetic disorder. This condition can lead to cardiac myxomas, skin pigmentation abnormalities, endocrine tumors, and other systemic manifestations. The test is performed on an EDTA blood sample using advanced Next Generation Sequencing for precise identification of pathogenic variants. Metropolis Healthcare provides accurate results to support early diagnosis, clinical management, and genetic counselling 

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

Price: Rs. 17,850.00

Sample Type: EDTA BLOOD

Fasting Not Required


Notes: G0099

Frequently Asked Questions (FAQ's):

What is Carney Complex?
Carney Complex is a rare genetic disorder caused by mutations in the PRKAR1A gene, leading to cardiac tumors, endocrine abnormalities, and skin pigmentation changes.

Which gene is tested in this panel?
The PRKAR1A gene is analyzed, as mutations in this gene are the primary cause of Carney Complex.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses high-precision NGS technology to detect point mutations, deletions, and duplications in the PRKAR1A gene.

What sample type is required?
An EDTA whole blood sample is needed for DNA extraction and sequencing.

Who should consider this test?
Individuals with cardiac myxomas, unusual skin pigmentation, endocrine tumors, or a family history of Carney Complex.

Is any preparation required before the test?
No fasting or special preparation is required.

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

How will the results help?
They confirm diagnosis, guide clinical management, and provide information for genetic counselling and family planning.

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