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DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E Genetic Test

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

-21%

The DNAJB6 gene plays a significant role in the development of limb-girdle muscular dystrophy, particularly the autosomal dominant type 1E (LGMD1E). This form of muscular dystrophy is characterized by progressive weakness and wasting of the limb-girdle muscles, which include the hips and shoulders. Mutations in the DNAJB6 gene disrupt its normal function, leading to the symptoms associated with LGMD1E.

To diagnose this specific type of muscular dystrophy, genetic testing is available at DNA Labs UAE. The test specifically looks for mutations in the DNAJB6 gene that are known to cause limb-girdle muscular dystrophy. This genetic test is crucial for accurate diagnosis, allowing for appropriate management and counseling for affected individuals and their families.

The cost of the DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E Genetic Test at DNA Labs UAE is 4400 AED. The test is performed using a sample of the patient’s blood, and the process involves analyzing the DNA to identify any mutations in the DNAJB6 gene. Results from this test can provide a definitive diagnosis, which is essential for understanding the prognosis and exploring potential treatment options.

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DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E Genetic Test

Components: DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E Genetic Test

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E

Test Details

The DNAJB6 gene is associated with limb-girdle muscular dystrophy, autosomal dominant type 1E (LGMD1E). This is a genetic disorder characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders and hips (limb-girdle muscles). It is inherited in an autosomal dominant pattern, meaning that an affected individual has a 50% chance of passing the gene mutation to each of their children.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations in an individual’s DNA. In the context of LGMD1E, NGS genetic testing can be used to identify mutations in the DNAJB6 gene, which can confirm a diagnosis of LGMD1E in an affected individual or identify individuals who carry the gene mutation but may not yet show symptoms.

NGS genetic testing can be helpful in diagnosing genetic disorders, providing information about disease progression and prognosis, and guiding treatment decisions. It can also be used for carrier testing, allowing individuals to determine if they carry a gene mutation that could be passed on to their children.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support before and after testing.

Test Name DNAJB6 Gene Limb-girdle muscular dystrophy autosomal dominant type 1E 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 DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DNAJB6 Gene Limb-girdle muscular dystrophy, autosomal dominant type 1E
Test Details

The DNAJB6 gene is associated with limb-girdle muscular dystrophy, autosomal dominant type 1E (LGMD1E). This is a genetic disorder characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders and hips (limb-girdle muscles). It is inherited in an autosomal dominant pattern, meaning that an affected individual has a 50% chance of passing the gene mutation to each of their children.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that can analyze multiple genes simultaneously to identify mutations or variations in an individual’s DNA. In the context of LGMD1E, NGS genetic testing can be used to identify mutations in the DNAJB6 gene, which can confirm a diagnosis of LGMD1E in an affected individual or identify individuals who carry the gene mutation but may not yet show symptoms.

NGS genetic testing can be helpful in diagnosing genetic disorders, providing information about disease progression and prognosis, and guiding treatment decisions. It can also be used for carrier testing, allowing individuals to determine if they carry a gene mutation that could be passed on to their children.

It’s important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support before and after testing.