Short Description

NGS genetic DNA test detecets for variant and mutation detection in UNC13D gene for Hemophagocytic lymphohistiocytosis type 3

PreTest Information

Clinical History of Patient who is going for UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test gene UNC13D

Detail Description

UNC13D Gene Hemophagocytic Lymphohistiocytosis Type 3 NGS Genetic DNA Test

Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening disorder that affects the immune system. It is characterized by an overactive immune system that leads to the destruction of healthy tissues and organs. Hemophagocytic lymphohistiocytosis type 3 is caused by mutations in the UNC13D gene. The UNC13D gene provides instructions for making a protein that is involved in the release of immune system cells called cytotoxic granules. Mutations in this gene can lead to a dysfunction in the immune system, resulting in hemophagocytic lymphohistiocytosis type 3.

Symptoms of Hemophagocytic Lymphohistiocytosis Type 3

The symptoms of hemophagocytic lymphohistiocytosis type 3 can be severe and life-threatening. They may include:

• Fever
• Enlarged liver and spleen
• Decreased blood cell counts
• Bleeding disorders
• Jaundice
• Neurological symptoms
• Organ failure

The symptoms of hemophagocytic lymphohistiocytosis type 3 can occur suddenly and progress rapidly. It is essential to seek medical attention immediately if you or someone you know experiences any of these symptoms.

Diagnosis of Hemophagocytic Lymphohistiocytosis Type 3

Diagnosing hemophagocytic lymphohistiocytosis type 3 can be challenging because it is a rare disorder. The diagnosis is usually made based on a combination of symptoms, physical examination, and laboratory tests. The laboratory tests may include blood tests, bone marrow biopsy, and genetic testing.

UNC13D Gene Hemophagocytic Lymphohistiocytosis Type 3 NGS Genetic DNA Test

The UNC13D gene hemophagocytic lymphohistiocytosis type 3 NGS genetic DNA test is a diagnostic test that can identify mutations in the UNC13D gene that cause hemophagocytic lymphohistiocytosis type 3. The test uses next-generation sequencing (NGS) technology to sequence the DNA of the UNC13D gene and identify any mutations that may be present.

Cost of the Test

The cost of the UNC13D gene hemophagocytic lymphohistiocytosis type 3 NGS genetic DNA test is INR 20,000. The cost may vary depending on the laboratory and location.

Conclusion

Hemophagocytic lymphohistiocytosis type 3 is a rare and life-threatening disorder caused by mutations in the UNC13D gene. The symptoms can be severe and progress rapidly, making early diagnosis and treatment essential. The UNC13D gene hemophagocytic lymphohistiocytosis type 3 NGS genetic DNA test is a diagnostic test that can identify mutations in the UNC13D gene and aid in the diagnosis of this disorder. If you or someone you know experiences any symptoms of hemophagocytic lymphohistiocytosis type 3, it is essential to seek medical attention immediately.

At DNA Labs India, we offer a wide range of genetic testing services, including the UNC13D gene hemophagocytic lymphohistiocytosis type 3 NGS genetic DNA test. Our team of experts uses state-of-the-art technology and techniques to provide accurate and reliable results. Contact us today to learn more about our services and how we can help you.

Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test