Short Description

NGS genetic DNA test detecets for variant and mutation detection in MYO5B gene for Diarrhea type 2 with microvillus atrophy

PreTest 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

Detail Description

MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy NGS Genetic DNA Test Cost INR 20000

Diarrhea is a common condition that affects people of all ages. However, there are certain types of diarrhea that are caused by genetic mutations. One such type is Diarrhea Type 2 with Microvillus Atrophy, which is caused by mutations in the MYO5B gene. This condition is also known as Microvillus Inclusion Disease (MVID).

Symptoms of Diarrhea Type 2 with Microvillus Atrophy

The symptoms of Diarrhea Type 2 with Microvillus Atrophy usually appear within a few days after birth. Infants with this condition experience chronic diarrhea, which can lead to dehydration and malnutrition. The diarrhea is usually severe, watery, and foul-smelling. Other symptoms of this condition include:

• Weight loss
• Failure to thrive
• Vomiting
• Abdominal distension
• Electrolyte imbalances

Diagnosis of Diarrhea Type 2 with Microvillus Atrophy

Diagnosis of Diarrhea Type 2 with Microvillus Atrophy can be challenging, as the symptoms can mimic other conditions. However, genetic testing can confirm the diagnosis. Next-Generation Sequencing (NGS) is a powerful tool that can identify mutations in the MYO5B gene. NGS is a type of genetic testing that can sequence millions of DNA fragments simultaneously. This allows for the detection of genetic mutations with high accuracy and speed.

MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy NGS Genetic DNA Test Cost

The cost of the MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy NGS Genetic DNA Test is INR 20000. This test is available at DNA Labs India, which is a leading provider of genetic testing services in India. DNA Labs India uses state-of-the-art technology and equipment to ensure accurate and reliable results.

Conclusion

Diarrhea Type 2 with Microvillus Atrophy is a rare genetic condition that can cause chronic diarrhea in infants. Genetic testing, such as the MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy NGS Genetic DNA Test, can confirm the diagnosis of this condition. DNA Labs India offers this test at an affordable cost, making it accessible to those who need it.

If you suspect that your child may have Diarrhea Type 2 with Microvillus Atrophy, it is important to seek medical attention as soon as possible. Early diagnosis and treatment can improve outcomes and prevent complications.

For more information on the MYO5B Gene Diarrhea Type 2 with Microvillus Atrophy NGS Genetic DNA Test, please contact DNA Labs India.