LCT Gene Lactase Deficiency Congenital Genetic Test
Test Name: LCT Gene Lactase Deficiency Congenital Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Metabolic Disorders
Doctor: General Physician
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for LCT Gene Lactase deficiency, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Lactase deficiency, congenital.
Test Details
LCT gene lactase deficiency, congenital is a genetic disorder that affects the ability to digest lactose, a sugar found in milk and dairy products. People with this condition have a deficiency of the enzyme lactase, which is needed to break down lactose into simpler sugars that can be absorbed by the body.
Congenital lactase deficiency is a rare genetic disorder that is typically diagnosed in infancy. Symptoms of the condition may include diarrhea, bloating, abdominal pain, and failure to thrive. The severity of symptoms can vary, with some individuals being able to tolerate small amounts of lactose while others may need to completely avoid lactose-containing foods.
Next-generation sequencing (NGS) genetic testing is a diagnostic tool used to identify genetic mutations or variations that may be associated with a particular condition. In the case of congenital lactase deficiency, NGS testing can be used to identify mutations in the LCT gene, which is responsible for producing the lactase enzyme.
NGS testing involves sequencing the entire DNA sequence of an individual’s genome or specific regions of interest. This allows for the detection of genetic variations that may be contributing to the development of a particular disorder. NGS testing can be more comprehensive and efficient compared to traditional genetic testing methods, as it can analyze multiple genes simultaneously.
NGS genetic testing for congenital lactase deficiency can provide valuable information for diagnosis, management, and genetic counseling. It can help confirm the presence of specific genetic mutations that cause the condition and guide treatment decisions, such as dietary modifications. Additionally, NGS testing can provide information about the inheritance pattern of the condition, which can be useful for family planning and genetic counseling.
It is important to note that NGS genetic testing for congenital lactase deficiency is typically performed by healthcare professionals, such as geneticists or genetic counselors, who are trained in interpreting and explaining the results to individuals and their families.
| Test Name | LCT Gene Lactase deficiency congenital 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for LCT Gene Lactase deficiency, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Lactase deficiency, congenital |
| Test Details |
LCT gene lactase deficiency, congenital is a genetic disorder that affects the ability to digest lactose, a sugar found in milk and dairy products. People with this condition have a deficiency of the enzyme lactase, which is needed to break down lactose into simpler sugars that can be absorbed by the body. Congenital lactase deficiency is a rare genetic disorder that is typically diagnosed in infancy. Symptoms of the condition may include diarrhea, bloating, abdominal pain, and failure to thrive. The severity of symptoms can vary, with some individuals being able to tolerate small amounts of lactose while others may need to completely avoid lactose-containing foods. Next-generation sequencing (NGS) genetic testing is a diagnostic tool used to identify genetic mutations or variations that may be associated with a particular condition. In the case of congenital lactase deficiency, NGS testing can be used to identify mutations in the LCT gene, which is responsible for producing the lactase enzyme. NGS testing involves sequencing the entire DNA sequence of an individual’s genome or specific regions of interest. This allows for the detection of genetic variations that may be contributing to the development of a particular disorder. NGS testing can be more comprehensive and efficient compared to traditional genetic testing methods, as it can analyze multiple genes simultaneously. NGS genetic testing for congenital lactase deficiency can provide valuable information for diagnosis, management, and genetic counseling. It can help confirm the presence of specific genetic mutations that cause the condition and guide treatment decisions, such as dietary modifications. Additionally, NGS testing can provide information about the inheritance pattern of the condition, which can be useful for family planning and genetic counseling. It is important to note that NGS genetic testing for congenital lactase deficiency is typically performed by healthcare professionals, such as geneticists or genetic counselors, who are trained in interpreting and explaining the results to individuals and their families. |
