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TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H Genetic Test

4,400 د.إ

-21%

The TRIM32 gene limb-girdle muscular dystrophy autosomal recessive type 2H genetic test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the TRIM32 gene. These mutations are responsible for causing limb-girdle muscular dystrophy type 2H (LGMD2H), a condition characterized by progressive weakness and wasting of the muscles around the hips and shoulders. This form of muscular dystrophy is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to develop the condition.

The test involves analyzing the patient’s DNA to search for specific genetic alterations in the TRIM32 gene that are known to cause LGMD2H. Early diagnosis through genetic testing is crucial for managing symptoms, implementing appropriate treatment plans, and providing genetic counseling for affected families.

DNA Labs UAE offers this comprehensive genetic test for a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by a team of expert geneticists and technicians, ensuring accurate and reliable results. Patients opting for this test can expect a thorough analysis of the TRIM32 gene, which will aid in confirming a diagnosis of limb-girdle muscular dystrophy type 2H, potentially guiding treatment decisions and helping to assess the risk of passing the condition on to future generations.

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TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H Genetic Test

Components: TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H 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 TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H.

Test Details: The TRIM32 gene is associated with limb-girdle muscular dystrophy, autosomal recessive type 2H (LGMD2H). This genetic disorder is characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders, upper arms, hips, and thighs. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of a person’s genes. In the context of LGMD2H, NGS genetic testing can be used to identify mutations or variations in the TRIM32 gene that may be responsible for the disorder. By analyzing the TRIM32 gene using NGS, healthcare professionals can provide a definitive diagnosis for LGMD2H and offer appropriate genetic counseling and management for affected individuals and their families. NGS testing can also be helpful in identifying carriers of the gene mutation, which can be important for family planning and reproductive decision-making. It is important to note that NGS genetic testing for LGMD2H should be performed by a qualified healthcare professional or genetic counselor, as they can provide appropriate pre- and post-test counseling, interpret the results accurately, and guide individuals and families in understanding the implications of the test results.

Test Name TRIM32 Gene Limb-girdle muscular dystrophy autosomal recessive type 2H 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 TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TRIM32 Gene Limb-girdle muscular dystrophy, autosomal recessive type 2H
Test Details

The TRIM32 gene is associated with limb-girdle muscular dystrophy, autosomal recessive type 2H (LGMD2H). This genetic disorder is characterized by progressive muscle weakness and wasting, primarily affecting the muscles of the shoulders, upper arms, hips, and thighs.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze the DNA sequence of a person’s genes. In the context of LGMD2H, NGS genetic testing can be used to identify mutations or variations in the TRIM32 gene that may be responsible for the disorder.

By analyzing the TRIM32 gene using NGS, healthcare professionals can provide a definitive diagnosis for LGMD2H and offer appropriate genetic counseling and management for affected individuals and their families. NGS testing can also be helpful in identifying carriers of the gene mutation, which can be important for family planning and reproductive decision-making.

It is important to note that NGS genetic testing for LGMD2H should be performed by a qualified healthcare professional or genetic counselor, as they can provide appropriate pre- and post-test counseling, interpret the results accurately, and guide individuals and families in understanding the implications of the test results.