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DLX5 Gene Split-Handfoot Malformation Type 1 with Sensorineural Hearing Loss Genetic Test Cost

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

-21%

The “DLX5 Gene Split-Hand/Foot Malformation Type 1 with Sensorineural Hearing Loss Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the DLX5 gene. These mutations are associated with Split-Hand/Foot Malformation Type 1 (SHFM1), a rare genetic disorder characterized by the malformation of the hands and feet, often presenting as a cleft or missing digits. Additionally, this test can detect if the genetic mutation has led to sensorineural hearing loss, a common complication associated with SHFM1.

The test is conducted through a detailed analysis of the patient’s DNA, extracted from a blood sample, to look for specific genetic alterations in the DLX5 gene that are known to cause the disorder. This genetic test is crucial for early diagnosis, allowing for better management and treatment planning for individuals affected by this condition.

At DNA Labs UAE, the cost of this comprehensive genetic test is 4400 AED. This investment covers the testing process, analysis, and a detailed report of the findings, which can be invaluable for affected families seeking to understand their condition and the potential for genetic counseling.

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DLX5 Gene Split-handfoot malformation type 1 with sensorineural hearing loss Genetic Test

Genetic testing can provide valuable insights into various genetic disorders, including DLX5 Gene Split-handfoot malformation type 1 with sensorineural hearing loss. At DNA Labs UAE, we offer a comprehensive genetic test that analyzes the DLX5 gene for specific mutations or variations associated with this condition.

Test Details

The DLX5 gene split-hand/foot malformation type 1 with sensorineural hearing loss NGS genetic test is a type of genetic test that utilizes next-generation sequencing (NGS) technology. This advanced technology allows us to accurately analyze the DLX5 gene and identify any variations or mutations that may be present.

Split-hand/foot malformation type 1 is a genetic disorder characterized by the absence or underdevelopment of certain fingers or toes, resulting in a split appearance. It can also affect the development of the limbs and other structures. Sensorineural hearing loss refers to a type of hearing loss caused by problems with the inner ear or the nerve pathways that transmit sound signals to the brain.

The DLX5 gene plays a crucial role in the development of limbs and the inner ear. Mutations or variations in this gene can disrupt normal development, leading to split-hand/foot malformation and sensorineural hearing loss. Our NGS genetic test for DLX5 gene mutations can help diagnose individuals with this condition.

Test Components and Price

Test Name: DLX5 Gene Split-handfoot malformation type 1 with sensorineural hearing loss Genetic Test

Components: NGS Technology

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Test Type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information

Prior to undergoing the DLX5 Gene Split-handfoot malformation type 1 with sensorineural hearing loss Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by this condition.

Interpreting the Results

It is crucial to interpret the results of the DLX5 gene test in the context of the individual’s clinical symptoms and family history. Genetic counseling is highly recommended to discuss the implications of the test results and any potential implications for the individual and their family members.

At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. Our DLX5 Gene Split-handfoot malformation type 1 with sensorineural hearing loss Genetic Test can aid in the diagnosis, genetic counseling, and treatment planning for individuals affected by this condition. Contact us today to learn more about our services and to schedule an appointment.

Test Name DLX5 Gene Split-handfoot malformation type 1 with sensorineural hearing loss 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 DLX5 Gene Split-hand/foot malformation type 1 with sensorineural hearing loss NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DLX5 Gene Split-hand/foot malformation type 1 with sensorineural hearing loss NGS Genetic DNA Test gene DLX5
Test Details

DLX5 gene split-hand/foot malformation type 1 with sensorineural hearing loss NGS genetic test is a type of genetic test that uses next-generation sequencing (NGS) technology to analyze the DLX5 gene for specific mutations or variations associated with split-hand/foot malformation type 1 (SHFM1) and sensorineural hearing loss.

Split-hand/foot malformation type 1 is a genetic disorder characterized by the absence or underdevelopment of certain fingers or toes, resulting in a split appearance. It can also affect the development of the limbs and other structures. Sensorineural hearing loss refers to a type of hearing loss caused by problems with the inner ear or the nerve pathways that transmit sound signals to the brain.

The DLX5 gene is involved in the development of limbs and the inner ear. Mutations or variations in this gene can disrupt normal development, leading to split-hand/foot malformation and sensorineural hearing loss.

The NGS genetic test for DLX5 gene mutations can help diagnose individuals with split-hand/foot malformation type 1 and sensorineural hearing loss. It involves sequencing the DNA of the individual to identify any variations or mutations in the DLX5 gene. This information can then be used to confirm the diagnosis, provide genetic counseling, and guide treatment options.

It is important to note that this genetic test is typically ordered by a healthcare professional who specializes in genetics or genetic counseling. The results of the test should be interpreted in the context of the individual’s clinical symptoms and family history. Genetic counseling is recommended to discuss the implications of the test results and any potential implications for the individual and their family members.

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