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FGD1 Gene Faciogenital Dysplasia Genetic Test Cost

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

-21%

The FGD1 Gene Faciogenital Dysplasia Genetic Test is a specialized diagnostic tool designed to identify mutations in the FGD1 gene, which are linked to the development of Faciogenital Dysplasia, also known as Aarskog-Scott syndrome. This rare genetic disorder is characterized by facial abnormalities, genital anomalies, and skeletal dysplasia, affecting predominantly males. The test is crucial for early diagnosis and management of the condition, enabling targeted interventions and genetic counseling for affected families.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or cheek swab. The laboratory utilizes advanced genomic technologies to analyze the FGD1 gene for any mutations that are known to cause the disorder. The results can provide invaluable insights for healthcare providers, helping to tailor treatment plans according to the specific needs of the patient.

The cost of the FGD1 Gene Faciogenital Dysplasia Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis and the detailed report provided by the lab, which includes interpretation of the results and recommendations for follow-up actions. Given the complexity of genetic disorders and the specialized technology required for accurate testing, the cost reflects the value of obtaining precise, personalized information that can significantly impact the patient’s quality of life and management of the condition.

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FGD1 Gene Faciogenital dysplasia Genetic Test

Cost: AED 4400.0

Test Components:

  • FGD1 Gene Faciogenital dysplasia Genetic Test

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 FGD1 Gene Faciogenital dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGD1 Gene Faciogenital dysplasia NGS Genetic DNA Test gene FGD1

Test Details:

The FGD1 gene, also known as faciogenital dysplasia 1 gene, is associated with a condition called faciogenital dysplasia (FGD). FGD is a rare genetic disorder that primarily affects the development of the face and external genitalia. NGS, or next-generation sequencing, is a genetic testing method that allows for the rapid and efficient sequencing of large amounts of DNA. NGS can be used to analyze the FGD1 gene to identify any genetic variants or mutations that may be present.

Genetic testing for FGD1 gene mutations can be helpful in diagnosing individuals with faciogenital dysplasia. It can also be used for carrier testing in individuals with a family history of the condition, as FGD is inherited in an autosomal recessive manner. By identifying specific genetic variants or mutations in the FGD1 gene, NGS genetic testing can provide valuable information for genetic counseling, family planning, and potential treatment options for individuals affected by faciogenital dysplasia.

Test Name FGD1 Gene Faciogenital dysplasia 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 FGD1 Gene Faciogenital dysplasia NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGD1 Gene Faciogenital dysplasia NGS Genetic DNA Test gene FGD1
Test Details

FGD1 gene, also known as faciogenital dysplasia 1 gene, is a gene that is associated with a condition called faciogenital dysplasia (FGD). FGD is a rare genetic disorder that primarily affects the development of the face and external genitalia.

NGS, or next-generation sequencing, is a genetic testing method that allows for the rapid and efficient sequencing of large amounts of DNA. NGS can be used to analyze the FGD1 gene to identify any genetic variants or mutations that may be present.

Genetic testing for FGD1 gene mutations can be helpful in diagnosing individuals with faciogenital dysplasia. It can also be used for carrier testing in individuals with a family history of the condition, as FGD is inherited in an autosomal recessive manner.

By identifying specific genetic variants or mutations in the FGD1 gene, NGS genetic testing can provide valuable information for genetic counseling, family planning, and potential treatment options for individuals affected by faciogenital dysplasia.

SKU: TEST-4105 Category:

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