KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test Cost
10,400.00 8,000.00 Book Test
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KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test Cost

10,400.00 8,000.00

-23%

KARYOTYPING FOR DETECTION OF Fragile X Syndrome genetic dna test done through Cytogenetics/Karyotyping sample type Peripheral Blood Sodium Heparin Vacutainer (2ml) Ambient reporting time for results 7-10days 8000

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Description

KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test Details:

What is Fragile X Syndrome?

Fragile X syndrome is the most common form of inherited intellectual disability in males and is also a significant cause of intellectual disability in females. It affects about 1 in 4,000 males and 1 in 8,000 females and occurs in all racial and ethnic groups.

Nearly all cases of fragile X syndrome are caused by an alteration (mutation) in the FMR1 gene where a DNA segment, known as the CGG triplet repeat, is expanded. Normally, this DNA segment is repeated from 5 to about 40 times. In people with fragile X syndrome, however, the CGG segment is repeated more than 200 times.

The abnormally expanded CGG segment inactivates (silences) the FMR1 gene, which prevents the gene from producing a protein called fragile X mental retardation protein. Loss of this protein leads to the signs and symptoms of fragile X syndrome. Both boys and girls can be affected, but because boys have only one X chromosome, a single fragile X is likely to affect them more severely.

Signs and Symptoms of Fragile X Syndrome:

A boy who has the full FMR1 mutation has fragile X syndrome and will have a moderate intellectual disability. They have a particular facial appearance, characterized by large head size, a long face, prominent forehead and chin and protruding ears. In addition, males who have fragile X syndrome have loose joints (joint laxity), and large testes (after puberty).

Affected boys may have behavioural problems such as hyperactivity, hand flapping, hand biting, temper tantrums and autism. Other behaviours in boys after they have reached puberty include poor eye contact, perseverative speech, problems in impulse control and distractibility. Physical problems that have been seen include eye, orthopaedic, heart and skin problems.

Girls who have the full FMR1 mutation have a mild intellectual disability. Family members who have fewer repeats in the FMR1 gene may not have an intellectual disability but may have other problems. Women with less severe changes may have premature menopause or difficulty becoming pregnant.

Diagnosis of Fragile X Syndrome:

DNA testing for fragile X syndrome is recommended. Karyotyping may reveal other chromosomal anomalies, and both a standard karyotype and DNA testing are suggested when a possible diagnosis of fragile X syndrome is considered.

The criterion standard diagnostic test involves molecular genetic techniques that detect the FMR1 gene. The exact number of CGG triplet repeats can be determined.  Southern blot and polymerase chain reaction (PCR) are the 2 methods of genetic analysis that are currently available.

Treatment of Fragile X Syndrome:

There is no specific treatment available for fragile X syndrome. Supportive therapy for children who have fragile X syndrome includes:

  • Special education and anticipatory management including avoidance of excessive stimulation to decrease behavioural problems.
  • Medication to manage behavioural issues, although no specific medication has been shown to be beneficial.
  • Early intervention, special education and vocational training.

Is Fragile X Syndrome Inherited?

This condition is inherited in an X-linked dominant pattern. A condition is considered X-linked if the mutated gene that causes the disorder is located on the X chromosome, one of the two sex chromosomes.

The inheritance is dominant if one copy of the altered gene in each cell is sufficient to cause the condition. In most cases, males experience more severe symptoms of the disorder than females. A striking characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons.

What is KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test?

KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test is a medical speciality that determines the cause and nature of diseases by examining and testing body tissues (Peripheral Blood Sodium Heparin Vacutainer 2ml Ambient). It is a KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test that screens for serious conditions.

What type of sample are needed to do a KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test?

A Peripheral Blood Sodium Heparin Vacutainer 2ml Ambient for testing can be obtained from several bodily sources. The cells are the most commonly tested are derived.

Standard Biological KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test Samples: Peripheral Blood Sodium Heparin Vacutainer 2ml Ambient

How accurate is KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test?

KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test is generally considered to be the most accurate testing method available. DNA Labs India’s KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test is considered as a benchmark by most doctors. The most precise and accurate KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test in India.

How many days does it take to obtain KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test results?

Results of KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test test are usually available from the laboratory within 1 week to 5 weeks.

For a standard KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test, DNA Labs India returns KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test results in 7 to 10 business days once all samples are received at the lab.

DNA Labs India understands that waiting for KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test results for this potentially life-changing test is stressful, so we provide speedy service without sacrificing accuracy.

Once complete, results are posted immediately to our secure online portal, and you will be notified by email right away.

Can KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test be done during pregnancy?

Prenatal KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test is a sensitive subject because of the ethical and legal issues involved, including the risks of an invasive test. You need to talk with your doctor.

How much does a KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test cost?

A standard KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test cost you 8000/- INR.

Why Choose DNA Labs India for KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test?

DNA labs India’s KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test follows with dual testing for 100% accuracy when determining a KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test.

  • We are the leading lab for KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test in India
  • Greater Accuracy
  • Collection centres across India
  • Outstanding customer service
  • Strict privacy and confidentiality assured
  • Full-service laboratories providing testing for use in complex cases

How to Schedule an Appointment for KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test?

You can either book online at the link provided. If you book and make the payment online free home collection service is provided to patients of all KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test.

How can I locate a KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test facility?

DNA labs India has 3000 plus sample collection centres across India for KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test.

You can choose the centre and book the KARYOTYPING FOR DETECTION OF Fragile X Syndrome Test online. For all online bookings made and payment paid a free home sample collection service is provided.

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