• Can I have this test done at home?

Yes, home sample collection is available through our platform for your convenience.

• What does a positive result mean?

A positive result indicates a genetic mutation was found, which helps confirm the diagnosis and guides hormone replacement therapy.

Kallmann Syndrome Genetic Test | Lahalak Medical Platform

Lahalak Medical PlatformDifferentiate Care

Medical notice: this information is for education and service understanding. It is not a diagnosis or a recommendation for an unnecessary procedure.

About this service

This molecular panel evaluates multiple genes involved in GnRH production and olfactory development, aiding the diagnosis of idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

Clinical Significance

Confirms the genetic diagnosis of Kallmann syndrome.
Identifies the specific mutation to guide clinical management.
Helps in assessing the risk of inheritance for future generations.

Genes Evaluated

KAL1 gene related to X-linked inheritance.
FGFR1 and PROKR2 receptor genes.
Multiple genes involved in GnRH neuron migration and olfactory development.

Indications for Testing

Patients presenting with delayed or absent puberty.
Individuals with anosmia or hyposmia (reduced smell).
Family history of idiopathic hypogonadotropic hypogonadism.

What is included?

✓Blood sample collection
✓Genetic sequencing analysis
✓Detailed medical result report

Conditions and notices

Fasting is not required
No special preparations are required before the test

Frequently Asked Questions

Short answers to the FAQs published with this service.

• What is Kallmann Syndrome?

It is a genetic condition characterized by a deficiency of reproductive hormones leading to delayed puberty, often combined with a diminished sense of smell.

• How is this genetic test performed?

The test is performed using a standard blood sample drawn from a vein; no invasive procedures are necessary.

• Is fasting required before the test?

No, fasting is not required for this genetic panel. You can eat and drink normally.

• How long does it take to get the results?

Due to the complexity of molecular sequencing, results typically take 14 to 21 working days.

Service resources and references

References and additional resources

Reference material and files associated with this service when available.

Scientific references

National Institutes of Health (NIH)
GeneReviews - Kallmann Syndrome

Kallmann Syndrome Genetic Screening

About this service

Clinical Significance

Genes Evaluated

Indications for Testing

What is included?

Conditions and notices

Frequently Asked Questions

References and additional resources

Scientific references

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