FKRP Gene Limb-girdle muscular dystrophy autosomal recessive type 2I Genetic Test
At DNA Labs UAE, we offer the FKRP Gene Limb-girdle muscular dystrophy autosomal recessive type 2I Genetic Test. This test helps diagnose and identify the causes of this genetic disorder.
Test Details
FKRP gene limb-girdle muscular dystrophy, autosomal recessive type 2I is a genetic disorder characterized by progressive muscle weakness and wasting. It is caused by mutations in the FKRP gene, which is involved in the glycosylation of alpha-dystroglycan, an important protein for muscle function.
Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously, providing accurate and comprehensive results. In the case of FKRP gene limb-girdle muscular dystrophy, autosomal recessive type 2I, this test involves sequencing the FKRP gene to identify any mutations or variations that may be causing the disorder.
This type of genetic test can help confirm a diagnosis of FKRP gene limb-girdle muscular dystrophy, autosomal recessive type 2I, and can also be used for carrier testing and prenatal diagnosis in families with a known mutation in the FKRP gene. It provides important information for genetic counseling and helps guide treatment and management decisions for individuals affected by the disorder.
Test Components and Price
Test Name: FKRP Gene Limb-girdle muscular dystrophy autosomal recessive type 2I Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Sample Condition
We accept blood samples, extracted DNA, or one drop of blood on FTA Card for this test.
Report Delivery
The test results will be delivered within 3 to 4 weeks after sample submission.
Test Type and Doctor
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department
Test Department: Genetics
Pre Test Information
Before undergoing the FKRP Gene Limb-girdle muscular dystrophy autosomal recessive type 2I NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with FKRP Gene Limb-girdle muscular dystrophy, autosomal recessive type 2I.
| Test Name | FKRP Gene Limb-girdle muscular dystrophy autosomal recessive type 2I Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card o |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Neurological Disorders |
| Doctor | Neurologist |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for FKRP Gene Limb-girdle muscular dystrophy, autosomal recessive type 2I NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FKRP Gene Limb-girdle muscular dystrophy, autosomal recessive type 2I |
| Test Details |
FKRP gene limb-girdle muscular dystrophy, autosomal recessive type 2I is a genetic disorder characterized by progressive muscle weakness and wasting. It is caused by mutations in the FKRP gene, which is involved in the glycosylation of alpha-dystroglycan, an important protein for muscle function. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of FKRP gene limb-girdle muscular dystrophy, autosomal recessive type 2I, an NGS genetic test would involve sequencing the FKRP gene to identify any mutations or variations that may be causing the disorder. This type of genetic test can help confirm a diagnosis of FKRP gene limb-girdle muscular dystrophy, autosomal recessive type 2I, and can also be used for carrier testing and prenatal diagnosis in families with a known mutation in the FKRP gene. It can provide important information for genetic counseling and help guide treatment and management decisions for individuals affected by the disorder. |
