Short Description

NGS genetic DNA test detecets for variant and mutation detection in CLMP gene for Congenital short-bowel syndrome

PreTest Information

Clinical History of Patient who is going for CLMP Gene Congenital short-bowel syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CLMP Gene Congenital short-bowel syndrome NGS Genetic DNA Test gene CLMP

Detail Description

CLMP Gene Congenital Short-Bowel Syndrome NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis - DNA Labs India

CLMP Gene Congenital Short-Bowel Syndrome is a rare genetic disorder that affects the digestive system. It is caused by a mutation in the CLMP gene, which is responsible for the development of the small intestine. This syndrome is characterized by a shortened small intestine, which leads to malabsorption of nutrients. The symptoms of this syndrome include diarrhea, vomiting, and weight loss. It is diagnosed using NGS Genetic DNA Test, which costs INR:20000.

At DNA Labs India, we offer advanced genetic testing services to diagnose CLMP Gene Congenital Short-Bowel Syndrome. Our NGS Genetic DNA Test is a powerful tool that can detect mutations in the CLMP gene with high accuracy. The test involves sequencing the DNA of the patient and comparing it to a reference genome to identify any mutations.

The cost of our NGS Genetic DNA Test for CLMP Gene Congenital Short-Bowel Syndrome is INR:20000. This includes the cost of sample collection, DNA sequencing, and interpretation of results. We provide detailed reports that explain the test results in a clear and concise manner, making it easy for patients and their families to understand the diagnosis.

If you suspect that you or your child may have CLMP Gene Congenital Short-Bowel Syndrome, it is important to get tested as soon as possible. Early diagnosis can help improve the outcome of the condition and prevent complications. Our experienced genetic counselors are available to guide you through the testing process and provide support throughout the diagnosis and treatment journey.

Contact DNA Labs India today to learn more about our NGS Genetic DNA Test for CLMP Gene Congenital Short-Bowel Syndrome and to schedule your appointment.

Congenital Short-Bowel Syndrome (CSBS) is a rare genetic disorder characterized by a shortened small intestine, which can result in difficulties absorbing nutrients and fluids from food. The CLMP gene (also known as CXADR-like membrane protein) has been associated with a form of CSBS. The CLMP gene provides instructions for producing a protein involved in cell adhesion and maintaining the integrity of tight junctions between cells in the intestines.

NGS (Next-Generation Sequencing) Genetic DNA Testing for the CLMP gene involves analyzing an individual's DNA to identify any mutations or variations that could be contributing to the development of Congenital Short-Bowel Syndrome related to CLMP gene mutations. Here's how the test typically works:

1. Sample Collection: A sample of the individual's DNA is collected, usually through a blood sample or saliva sample.

2. DNA Sequencing: Next-Generation Sequencing technology is used to analyze the DNA. This technology allows for the rapid and comprehensive sequencing of multiple genes simultaneously.

3. Genetic Analysis: The DNA sequence of the CLMP gene is compared to a reference sequence to identify any differences, mutations, or variations.

4. Variant Interpretation: Any identified genetic variants are interpreted by medical professionals. Variants that are known to be associated with Congenital Short-Bowel Syndrome caused by CLMP gene mutations or other genetic conditions are considered significant.

5. Clinical Correlation: The genetic test results are interpreted in the context of the individual's clinical presentation, symptoms, and medical history.

6. Genetic Counseling: The individual and their family are provided with genetic counseling to understand the implications of the test results, potential inheritance patterns, and medical management.

Genetic testing for Congenital Short-Bowel Syndrome related to CLMP gene mutations can be important for confirming a diagnosis, understanding the underlying genetic cause, and guiding treatment and management strategies. It's important to note that genetic testing is a complex process, and the interpretation of results requires specialized medical expertise.

If you or someone you know is considering undergoing NGS Genetic DNA Testing for Congenital Short-Bowel Syndrome related to CLMP gene mutations, it's recommended to consult with a pediatric gastroenterologist, medical geneticist, genetic counselor, or healthcare provider who specializes in gastrointestinal disorders and genetic conditions. They can provide guidance on whether genetic testing is appropriate, the potential implications of the results, and any available treatments or management strategies.