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FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test Cost

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

-21%

The FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the FLVCR2 gene, which are associated with Fowler syndrome. Fowler syndrome is a rare genetic condition characterized by hydranencephaly, where the brain’s cerebral hemispheres are largely absent and replaced with sacs filled with cerebrospinal fluid. This condition is typically fatal, and affected infants often have a poor prognosis.

The test is crucial for early detection and understanding of the genetic underpinnings of this condition, enabling healthcare providers to offer accurate genetic counseling to affected families. By examining the FLVCR2 gene, this test can confirm a diagnosis of Fowler syndrome, helping in the management and planning for the care of affected individuals.

The cost of the FLVCR2 Gene Hydranencephaly Fowler Type Genetic Test at DNA Labs UAE is set at 4400 AED. This investment includes the comprehensive analysis necessary to identify the specific mutations within the FLVCR2 gene that are indicative of Fowler syndrome. DNA Labs UAE is equipped with state-of-the-art genetic testing technology and staffed by professionals skilled in the interpretation of genetic data, ensuring that patients and their families receive accurate and meaningful results.

Description

FLVCR2 Gene Hydranencephaly Fowler type Genetic Test

Components: FLVCR2 Gene Hydranencephaly Fowler type 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: Clinical History of Patient who is going for FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic DNA Test gene FLVCR2.

Test Details: The FLVCR2 gene is associated with a rare neurological disorder called hydranencephaly, Fowler type. Hydranencephaly is characterized by the absence of cerebral hemispheres and the presence of fluid-filled sacs in the skull. This condition leads to severe developmental delays and neurological impairments.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the FLVCR2 gene for any mutations or variations that may be associated with hydranencephaly, Fowler type. NGS is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes, providing a comprehensive view of the individual’s genetic makeup.

By identifying any mutations or variations in the FLVCR2 gene, NGS genetic testing can help in the diagnosis and management of hydranencephaly, Fowler type. It can also provide valuable information for genetic counseling and family planning.

It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the results.

Test Name	FLVCR2 Gene Hydranencephaly Fowler type 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 FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FLVCR2 Gene Hydranencephaly, Fowler type NGS Genetic DNA Test gene FLVCR2
Test Details	The FLVCR2 gene is associated with a rare neurological disorder called hydranencephaly, Fowler type. Hydranencephaly is characterized by the absence of cerebral hemispheres and the presence of fluid-filled sacs in the skull. This condition leads to severe developmental delays and neurological impairments. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the FLVCR2 gene for any mutations or variations that may be associated with hydranencephaly, Fowler type. NGS is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes, providing a comprehensive view of the individual’s genetic makeup. By identifying any mutations or variations in the FLVCR2 gene, NGS genetic testing can help in the diagnosis and management of hydranencephaly, Fowler type. It can also provide valuable information for genetic counseling and family planning. It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the results.