Sale!

GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependant Diabetes Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependent Diabetes Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the GFM2 gene. This gene has been associated with a rare but severe condition characterized by microcephaly (a smaller than normal head size), a simplified gyral pattern of the brain, and insulin-dependent diabetes. These symptoms represent a complex neurodevelopmental disorder that can significantly impact the affected individual’s quality of life.

The test involves analyzing the patient’s DNA to identify any genetic alterations in the GFM2 gene that could lead to the development of these conditions. It is particularly crucial for early diagnosis and management of the symptoms, especially for guiding treatment options for the insulin-dependent diabetes component of the disorder.

DNA Labs UAE offers this genetic test at a cost of 4400 AED. The laboratory is equipped with state-of-the-art technology to ensure accurate and reliable results. By opting for this test, patients and their families can gain valuable insights into their genetic makeup, enabling informed decisions regarding their health and medical care. This test is especially recommended for individuals with a family history of the condition or those exhibiting symptoms related to the disorder.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependent Diabetes Genetic Test

Welcome to DNA Labs UAE, where we offer the GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependent Diabetes Genetic Test. This test is designed to diagnose and provide information about a condition associated with the GFM2 gene. Read on to learn more about the symptoms, diagnosis, test components, price, sample condition, report delivery, method, test type, doctor, test department, pre-test information, and test details.

Test Name: GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependent Diabetes Genetic Test

  • Components: Dysmorphology
  • 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: Genetics
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the GFM2 Gene Microcephaly with Simplified Gyral Pattern and Insulin-Dependent Diabetes Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the condition.

Test Details

The GFM2 gene is associated with a condition known as microcephaly with simplified gyral pattern and insulin-dependent diabetes. Microcephaly refers to a smaller than average head size, while simplified gyral pattern refers to a less complex folding pattern of the brain’s surface. Insulin-dependent diabetes, also known as type 1 diabetes, is a condition where the body’s immune system mistakenly attacks and destroys the insulin-producing cells in the pancreas.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the identification of genetic variations or mutations that may be responsible for a particular condition or disease. In the context of GFM2 gene-related microcephaly with simplified gyral pattern and insulin-dependent diabetes, NGS genetic testing can be used to analyze the GFM2 gene for any mutations or variations that may be present. This can help in confirming a diagnosis, understanding the genetic cause of the condition, and providing information for genetic counseling and management of the condition.

It is important to consult with a healthcare professional or a genetic counselor for more information and guidance regarding NGS genetic testing and its implications for the specific condition mentioned.

Test Name GFM2 Gene Microcephaly with symplified gyral pattern and insulin-dependant diabetes 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GFM2 Gene Microcephaly with symplified gyral pattern and insulin-dependant diabetes NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GFM2 Gene Microcephaly with symplified gyral pattern and insulin-dependant diabetes NGS Genetic DNA Test gene GFM2
Test Details

The GFM2 gene is associated with a condition called microcephaly with simplified gyral pattern and insulin-dependent diabetes. Microcephaly refers to a smaller than average head size, while simplified gyral pattern refers to a less complex folding pattern of the brain’s surface. Insulin-dependent diabetes, also known as type 1 diabetes, is a condition where the body’s immune system mistakenly attacks and destroys the insulin-producing cells in the pancreas.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the identification of genetic variations or mutations that may be responsible for a particular condition or disease.

In the context of GFM2 gene-related microcephaly with simplified gyral pattern and insulin-dependent diabetes, NGS genetic testing can be used to analyze the GFM2 gene for any mutations or variations that may be present. This can help in confirming a diagnosis, understanding the genetic cause of the condition, and providing information for genetic counseling and management of the condition.

It’s important to consult with a healthcare professional or a genetic counselor for more information and guidance regarding NGS genetic testing and its implications for the specific condition mentioned.