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ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test Cost

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

-21%

The ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the ALX3 gene, which are known to cause Frontonasal Dysplasia Type 1. This condition is a rare genetic disorder characterized by a spectrum of abnormalities affecting the development of the head and face, often leading to distinct facial features, including a widened nasal bridge, a broad nose tip, and, in some cases, cleft lip and palate. The test is crucial for early diagnosis, allowing for appropriate management and counseling of affected individuals and their families. With a cost of 4400 AED, the test represents a significant step forward in the field of genetic diagnostics, providing insights into a complex condition and offering hope for affected families seeking understanding and support.

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ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test

At DNA Labs UAE, we offer the ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test. This test helps in diagnosing and understanding Frontonasal Dysplasia Type 1 (FND1), a rare genetic disorder characterized by abnormalities of the head and face.

Test Details

The ALX3 gene is associated with FND1. This condition is characterized by abnormalities such as a wide or bifid nasal tip, cleft lip and/or palate, hypertelorism (increased distance between the eyes), and malformations of the forehead and skull.

Our ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test uses NGS (Next-Generation Sequencing) technology. This allows for the simultaneous analysis of multiple genes, including the ALX3 gene. By analyzing this gene, we can determine if there are any mutations or variants present that may be responsible for the condition.

Test Components and Price

The cost of the ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test is 4400.0 AED.

Sample Condition

We accept blood samples, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Test Type

The ALX3 Gene Frontonasal Dysplasia Type 1 Genetic Test falls under the category of Dysmorphology.

Doctor and Test Department

This test is conducted by our qualified Pediatrics doctor and is performed in our Genetics department.

Pre Test Information

Prior to the test, we require the clinical history of the patient who is going for the ALX3 Gene Frontonasal Dysplasia Type 1 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by the ALX3 gene.

Importance of Genetic Testing

NGS genetic testing can help confirm a diagnosis of FND1 in individuals with suspected symptoms. It can also identify carriers of the condition within a family and provide information about the specific genetic variant involved. This information can be useful for genetic counseling and family planning.

It’s important to note that genetic testing for FND1 should be performed by a qualified healthcare professional or genetic counselor. They can interpret the results and provide appropriate guidance and support.

Test Name ALX3 Gene Frontonasal dysplasia type 1 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 ALX3 Gene Frontonasal dysplasia type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ALX3 Gene Frontonasal dysplasia type 1 NGS Genetic DNA Test gene ALX3
Test Details

The ALX3 gene is associated with a condition called frontonasal dysplasia type 1 (FND1). FND1 is a rare genetic disorder characterized by abnormalities of the head and face. These abnormalities may include a wide or bifid nasal tip, cleft lip and/or palate, hypertelorism (increased distance between the eyes), and malformations of the forehead and skull.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes. In the case of FND1, NGS can be used to analyze the ALX3 gene to determine if there are any mutations or variants present that may be responsible for the condition.

NGS genetic testing can help confirm a diagnosis of FND1 in individuals with suspected symptoms, as well as identify carriers of the condition within a family. It can also provide information about the specific genetic variant involved, which can be useful for genetic counseling and family planning.

It’s important to note that genetic testing for FND1 should be performed by a qualified healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance and support.

SKU: TEST-4116 Category:

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