4H SYNDROME GENE PANEL BY NGS, EDTA BLOOD

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NABL Cap Accredited     
The 4H Syndrome Gene Panel by NGS analyzes genes associated with 4H syndrome, a rare genetic disorder characterized by hypomyelination, hypodontia, and hypogonadotropic hypogonadism. Identifying pathogenic variants aids in accurate diagnosis, prognosis, and genetic counseling. Metropolis Healthcare performs this panel using next-generation sequencing (NGS) on EDTA blood samples, ensuring high precision and reliable detection of mutations. It is recommended for individuals presenting with neurological deficits, developmental delays, or hormonal abnormalities suggestive of 4H syndrome. Results from Metropolis Healthcare support informed clinical management and family planning

  • 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: G0162

Frequently Asked Questions (FAQ's):

What does the 4H Syndrome Gene Panel detect at Metropolis Healthcare?
It identifies genetic mutations associated with 4H syndrome for precise diagnosis.

Why is this test important at Metropolis Healthcare?
It provides definitive diagnosis, informs prognosis, and guides genetic counseling.

Who should take this test at Metropolis Healthcare?
Individuals with developmental delays, hypomyelination, hormonal abnormalities, or suspected 4H syndrome.

How does Metropolis Healthcare perform the 4H Syndrome Gene Panel?
Using next-generation sequencing (NGS) technology for sensitive and accurate detection of pathogenic variants.

What sample type is required at Metropolis Healthcare?
EDTA blood collected through routine venipuncture is required.

Is any special preparation needed before the test at Metropolis Healthcare?
No fasting or special preparation is necessary.

How long does it take to receive results from Metropolis Healthcare?
Results are usually available within the standard NGS reporting timeframe.

Can Metropolis Healthcare provide follow-up after testing?
Yes, guidance on management, treatment planning, and genetic counseling is available

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