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MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test Cost

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

-21%

The “MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the MYO5B gene. These mutations are known to cause a rare but severe disorder characterized by diarrhea and microvillus atrophy, a condition where the microscopic hair-like structures (microvilli) that line the intestine and aid in nutrient absorption are absent or abnormal. This genetic test is crucial for early diagnosis and management of the condition, which can significantly impact a patient’s quality of life. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed. By identifying the genetic basis of the disorder, healthcare providers can tailor treatment plans more effectively, offering hope to affected individuals and their families.

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MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test

At DNA Labs UAE, we offer the MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test. This test helps in diagnosing and understanding a rare genetic disorder called microvillus inclusion disease (MVID). The test is performed using Next-Generation Sequencing (NGS) technology, which allows for a comprehensive analysis of an individual’s genetic makeup.

Test Components and Price

The MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test costs AED 4400.0. The test requires a blood sample or extracted DNA, or even just one drop of blood on an FTA card.

Report Delivery and Method

The report for the MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test is typically delivered within 3 to 4 weeks. The test is conducted using NGS technology, which ensures accurate and reliable results.

Test Type and Doctor

The MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test falls under the category of Osteology Dermatology Immunology Disorders. This test is usually recommended by dermatologists. The test is performed in our Genetics department.

Pre Test Information

Prior to undergoing the MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by this disorder.

Test Details

The MYO5B gene is associated with microvillus inclusion disease (MVID), a rare genetic disorder. Individuals with MVID experience severe diarrhea from birth and throughout their lives. This disorder is caused by mutations in the MYO5B gene, which is responsible for protein transport within cells.

NGS genetic testing allows for the analysis of the MYO5B gene to identify any mutations or variations. This type of testing provides a comprehensive view of an individual’s genetic makeup by simultaneously analyzing multiple genes.

By performing NGS genetic testing, specific mutations in the MYO5B gene associated with diarrhea type 2 with microvillus atrophy can be identified. This helps in confirming the diagnosis and determining the specific mutation in the MYO5B gene. This information is valuable for genetic counseling, family planning, and potentially guiding treatment options.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy Genetic Test can help in the diagnosis and management of this rare genetic disorder.

Test Name MYO5B Gene Diarrhea type 2 with microvillus atrophy 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MYO5B Gene Diarrhea type 2 with microvillus atrophy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MYO5B Gene Diarrhea type 2 with microvillus atrophy NGS Genetic DNA Test gene MYO5B
Test Details

The MYO5B gene is associated with a rare genetic disorder called microvillus inclusion disease (MVID). MVID is characterized by severe diarrhea that begins shortly after birth and persists throughout life. This disorder is caused by mutations in the MYO5B gene, which is involved in the transport of proteins within cells.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the MYO5B gene for any mutations or variations. This type of testing allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. NGS can identify specific mutations in the MYO5B gene that are associated with diarrhea type 2 with microvillus atrophy.

If a person is suspected of having this disorder, NGS genetic testing can help confirm the diagnosis and identify the specific mutation in the MYO5B gene. This information can be valuable for genetic counseling, family planning, and potentially guiding treatment options.

SKU: TEST-2922 Category:

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