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FLNB Gene Larsen Syndrome Genetic Test Cost

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

-21%

The FLNB Gene Larsen Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the FLNB gene, which are associated with Larsen syndrome. Larsen syndrome is a rare genetic disorder characterized by congenital abnormalities including dislocations of the hips, knees, and elbows, along with distinctive facial features and other skeletal anomalies. The test plays a crucial role in the early diagnosis and management of the syndrome, enabling healthcare providers to devise appropriate treatment and intervention strategies.

Priced at 4400 AED, the test involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the FLNB gene. The results from this test can provide valuable information for affected individuals and their families regarding the condition, its inheritance pattern, and the risk of passing it on to future generations. Conducted at DNA Labs UAE, the test is performed by experienced geneticists and laboratory technicians who ensure accuracy and confidentiality of the results.

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FLNB Gene Larsen Syndrome Genetic Test

At DNA Labs UAE, we offer the FLNB Gene Larsen Syndrome Genetic Test to help diagnose and manage this rare genetic disorder. This blog will provide detailed information about the test, including its components, cost, symptoms, diagnosis, and more.

Test Details

The FLNB gene is responsible for producing the protein filamin B, which plays a crucial role in the structure and function of cells. Mutations in the FLNB gene can lead to Larsen syndrome, a rare genetic disorder characterized by multiple joint dislocations, abnormal curvature of the spine (kyphoscoliosis), and other skeletal abnormalities.

Components

  • Test Name: FLNB Gene Larsen Syndrome 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the FLNB Gene Larsen Syndrome 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 the FLNB Gene Larsen Syndrome NGS Genetic DNA Test gene FLNB.

Test Process

Next-generation sequencing (NGS) genetic testing is utilized to analyze the DNA sequence of multiple genes simultaneously. This allows for the identification of genetic variations or mutations in the FLNB gene, which can aid in diagnosing Larsen syndrome. The process involves obtaining a DNA sample, typically through a blood or saliva sample, and sequencing the genetic material to identify any changes or mutations in the FLNB gene.

Benefits of Genetic Testing

Genetic testing for Larsen syndrome can provide several benefits, including:

  • Confirming a diagnosis
  • Providing accurate genetic counseling
  • Guiding appropriate medical management and treatment options
  • Carrier testing in family members
  • Prenatal testing in pregnancies at risk of inheriting the condition

By undergoing the FLNB Gene Larsen Syndrome Genetic Test, individuals and families can gain a better understanding of the condition and make informed decisions regarding their healthcare.

If you suspect that you or a family member may have Larsen syndrome, we encourage you to consult with a healthcare professional and consider genetic testing. At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services to assist in the diagnosis and management of genetic disorders.

Test Name FLNB Gene Larsen syndrome 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 FLNB Gene Larsen syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FLNB Gene Larsen syndrome NGS Genetic DNA Test gene FLNB
Test Details

The FLNB gene is responsible for producing the protein filamin B, which plays a crucial role in the structure and function of cells. Mutations in the FLNB gene can lead to a rare genetic disorder known as Larsen syndrome.

Larsen syndrome is characterized by multiple joint dislocations, abnormal curvature of the spine (kyphoscoliosis), and other skeletal abnormalities. It is an autosomal dominant disorder, meaning that an individual only needs to inherit one copy of the mutated FLNB gene from either parent to develop the condition.

Next-generation sequencing (NGS) genetic testing is a method used to analyze the DNA sequence of multiple genes simultaneously. It allows for the identification of genetic variations or mutations in the FLNB gene, which can help diagnose Larsen syndrome.

NGS testing involves obtaining a DNA sample, usually through a blood or saliva sample, and sequencing the genetic material to identify any changes or mutations in the FLNB gene. This information can be used to confirm a diagnosis of Larsen syndrome and provide information about the specific genetic variant causing the condition.

Genetic testing for Larsen syndrome can be helpful in confirming a diagnosis, providing accurate genetic counseling, and guiding appropriate medical management and treatment options. It may also be used for carrier testing in family members or prenatal testing in pregnancies at risk of inheriting the condition.

SKU: TEST-4201 Category:

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