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SPINT2 Gene Diarrhea type 3 secretory sodium congenital syndromic Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The SPINT2 Gene Diarrhea Type 3 Secretory Sodium Congenital Syndromic Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE. This test specifically targets the analysis of the SPINT2 gene, which has been associated with a rare congenital disorder characterized by severe secretory diarrhea and various syndromic features. The condition, often referred to as Congenital Sodium Diarrhea (CSD), is a result of mutations in the SPINT2 gene that affect the body’s ability to properly absorb and regulate sodium, leading to significant electrolyte imbalances and dehydration.

The genetic test aims to identify mutations within the SPINT2 gene to confirm a diagnosis of this type of congenital diarrheal disorder. Early identification of the condition can significantly improve the management and treatment options for affected individuals, helping to mitigate some of the more severe symptoms and improve quality of life.

The cost of the SPINT2 Gene Diarrhea Type 3 Secretory Sodium Congenital Syndromic Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted with state-of-the-art genetic sequencing technologies to ensure accurate and reliable results. Families who have a history of congenital diarrhea or syndromic features that may be linked to sodium imbalance are encouraged to consider this test for early detection and intervention.

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SPINT2 Gene Diarrhea type 3 secretory sodium congenital syndromic Genetic Test

Test Details

The SPINT2 gene is associated with a condition called Diarrhea type 3, secretory sodium, congenital, syndromic. This genetic test is a Next-Generation Sequencing (NGS) test that analyzes the SPINT2 gene for any mutations or variations that may be present.

Diarrhea type 3, secretory sodium, congenital, syndromic is a rare genetic disorder that affects the intestines and causes chronic diarrhea. This condition is typically present from birth and is characterized by excessive secretion of sodium in the intestines, leading to the loss of water and electrolytes and resulting in diarrhea.

The NGS genetic test for SPINT2 gene mutations can help in the diagnosis of this condition. It involves sequencing the DNA of an individual to identify any changes or variations in the SPINT2 gene that may be responsible for the disorder. This test can provide valuable information for healthcare professionals in determining the underlying cause of the symptoms and guiding appropriate treatment options.

It is important to note that this genetic test is specific to the SPINT2 gene and may not detect mutations in other genes that could also cause similar symptoms. Genetic counseling is recommended for individuals considering this test to better understand the implications and limitations of the results.

Test Name

SPINT2 Gene Diarrhea type 3 secretory sodium congenital syndromic Genetic Test

Components

Price: 4400.0 AED

Sample Condition

Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

3 to 4 Weeks

Method

NGS Technology

Test Type

Metabolic Disorders

Doctor

General Physician

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for SPINT2 Gene Diarrhea type 3, secretory sodium, congenital, syndromic NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Diarrhea type 3, secretory sodium, congenital, syndromic

Test Name SPINT2 Gene Diarrhea type 3 secretory sodium congenital syndromic Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SPINT2 Gene Diarrhea type 3, secretory sodium, congenital, syndromic NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Diarrhea type 3, secretory sodium, congenital, syndromic
Test Details

The SPINT2 gene is associated with a condition called Diarrhea type 3, secretory sodium, congenital, syndromic. This genetic test is a Next-Generation Sequencing (NGS) test that analyzes the SPINT2 gene for any mutations or variations that may be present.

Diarrhea type 3, secretory sodium, congenital, syndromic is a rare genetic disorder that affects the intestines and causes chronic diarrhea. This condition is typically present from birth and is characterized by excessive secretion of sodium in the intestines, leading to the loss of water and electrolytes and resulting in diarrhea.

The NGS genetic test for SPINT2 gene mutations can help in the diagnosis of this condition. It involves sequencing the DNA of an individual to identify any changes or variations in the SPINT2 gene that may be responsible for the disorder. This test can provide valuable information for healthcare professionals in determining the underlying cause of the symptoms and guiding appropriate treatment options.

It is important to note that this genetic test is specific to the SPINT2 gene and may not detect mutations in other genes that could also cause similar symptoms. Genetic counseling is recommended for individuals considering this test to better understand the implications and limitations of the results.

SKU: TEST-2291 Category:

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