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MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant Genetic Test Cost

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

-21%

The MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE. Priced at 4400 AED, this test is designed to identify mutations in the MEOX1 gene, which are associated with Klippel-Feil Syndrome Type 2 (KFS2). KFS2 is a rare genetic disorder characterized by the congenital fusion of any two of the seven cervical vertebrae. It is part of a broader spectrum of disorders affecting spinal segmentation and alignment, leading to a range of symptoms from mild neck stiffness to more severe neurological complications due to spinal cord or nerve root involvement.

The test is aimed at individuals who exhibit symptoms of KFS2 or have a family history of the condition, offering them a precise genetic diagnosis. By confirming the presence of a mutation in the MEOX1 gene, the test can help in the development of a tailored management plan for the affected individual. It is also valuable for families seeking information on the risk of passing the condition to future generations, given its autosomal dominant inheritance pattern. Conducted at the state-of-the-art facilities of DNA Labs UAE, the test ensures accuracy and reliability, providing essential genetic insights for affected individuals and their families.

Description

MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant Genetic Test

Test Name: MEOX1 Gene Klippel-Feil Syndrome Type 2 Autosomal Dominant Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 MEOX1 Gene Klippel-Feil Syndrome Type 2, Autosomal Dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MEOX1 Gene Klippel-Feil Syndrome Type 2, Autosomal Dominant NGS Genetic DNA Test gene MEOX1

Test Details:

MEOX1 gene is not directly associated with Klippel-Feil Syndrome Type 2. Klippel-Feil Syndrome is a rare genetic disorder characterized by the fusion of two or more cervical vertebrae, leading to a limited range of motion in the neck and other associated abnormalities.

The genetic causes of Klippel-Feil Syndrome are not fully understood, but mutations in various genes have been identified in some individuals with the condition. These genes include GDF6, GDF3, MEOX1, and MYO18B, among others. However, the exact role of these genes in the development of Klippel-Feil Syndrome is still being studied.

NGS (Next-Generation Sequencing) genetic testing is a powerful tool used to analyze multiple genes simultaneously and identify genetic variants that may be associated with a particular condition. However, it is important to note that NGS panels for Klippel-Feil Syndrome typically include multiple genes, not just MEOX1, as the exact genetic cause can vary among individuals.

If you suspect you or someone you know may have Klippel-Feil Syndrome, it is recommended to consult with a geneticist or a healthcare professional who specializes in genetic disorders for a comprehensive evaluation and appropriate genetic testing. They can guide you through the testing process and provide personalized information and support.

Test Name	MEOX1 Gene Klippel-Feil syndrome type 2 autosomal dominant 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 MEOX1 Gene Klippel-Feil syndrome type 2, autosomal dominant NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MEOX1 Gene Klippel-Feil syndrome type 2, autosomal dominant NGS Genetic DNA Test gene MEOX1
Test Details	MEOX1 gene is not directly associated with Klippel-Feil syndrome type 2. Klippel-Feil syndrome is a rare genetic disorder characterized by the fusion of two or more cervical vertebrae, leading to a limited range of motion in the neck and other associated abnormalities. The genetic causes of Klippel-Feil syndrome are not fully understood, but mutations in various genes have been identified in some individuals with the condition. These genes include GDF6, GDF3, MEOX1, and MYO18B, among others. However, the exact role of these genes in the development of Klippel-Feil syndrome is still being studied. NGS (Next-Generation Sequencing) genetic testing is a powerful tool used to analyze multiple genes simultaneously and identify genetic variants that may be associated with a particular condition. However, it is important to note that NGS panels for Klippel-Feil syndrome typically include multiple genes, not just MEOX1, as the exact genetic cause can vary among individuals. If you suspect you or someone you know may have Klippel-Feil syndrome, it is recommended to consult with a geneticist or a healthcare professional who specializes in genetic disorders for a comprehensive evaluation and appropriate genetic testing. They can guide you through the testing process and provide personalized information and support.