Short Description

NGS genetic DNA test detecets for variant and mutation detection in CLDN19 gene for Hypomagnesemia type 5

PreTest Information

Clinical History of Patient who is going for CLDN19 Gene Hypomagnesemia type 5 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypomagnesemia type 5

Detail Description

CLDN19 Gene Hypomagnesemia Type 5 NGS Genetic DNA Test Cost INR 20000: Symptoms and Diagnosis

Hypomagnesemia is a condition characterized by low levels of magnesium in the blood. Magnesium is an important mineral that plays a crucial role in various bodily functions such as nerve and muscle function, heart rhythm, and bone health.

There are various types of hypomagnesemia, including Hypomagnesemia type 5, which is caused by mutations in the CLDN19 gene. This gene provides instructions for making a protein that helps regulate the movement of magnesium in the kidneys.

Symptoms of Hypomagnesemia Type 5

The symptoms of Hypomagnesemia type 5 can vary depending on the severity of the condition. Some common symptoms include:

• Muscle weakness and cramps
• Tremors
• Numbness and tingling in the extremities
• Seizures
• Abnormal heart rhythms
• Developmental delays in children

Diagnosis of Hypomagnesemia Type 5

A diagnosis of Hypomagnesemia type 5 can be made through genetic testing. Next-generation sequencing (NGS) is a type of genetic testing that can analyze multiple genes at once. This type of testing can be particularly useful for identifying rare genetic conditions such as Hypomagnesemia type 5.

The NGS genetic DNA test for Hypomagnesemia type 5 typically costs around INR 20000 in India. This test involves collecting a blood or saliva sample from the patient and sending it to a laboratory for analysis.

If a mutation in the CLDN19 gene is identified through genetic testing, additional testing may be needed to determine the extent of the condition and develop an appropriate treatment plan.

Conclusion

Hypomagnesemia type 5 is a rare genetic condition that can cause a range of symptoms. Genetic testing, such as NGS, can be useful for diagnosing this condition and developing an appropriate treatment plan. If you or a loved one is experiencing symptoms of Hypomagnesemia type 5, it is important to speak with a healthcare provider and consider genetic testing.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS for Hypomagnesemia type 5. Contact us today to learn more about our services and how we can help.