Sale!

FOXF2 Gene Disorders of sex development with cleft palate Genetic Test Cost

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

-21%

The “FOXF2 Gene Disorders of Sex Development with Cleft Palate Genetic Test” is a specialized diagnostic evaluation available at DNA Labs UAE, designed to identify genetic abnormalities associated with disorders of sex development (DSD) and cleft palate that are linked to mutations in the FOXF2 gene. This gene plays a crucial role in embryonic development, including the development of the reproductive system and facial structures. Mutations in the FOXF2 gene can lead to a spectrum of developmental issues, notably affecting sex differentiation and causing cleft palate, a condition characterized by a split in the roof of the mouth.

This test is particularly valuable for individuals presenting with symptoms of DSD and cleft palate, families with a history of these conditions, or healthcare providers seeking a genetic explanation for these developmental anomalies in their patients. By analyzing the DNA for specific mutations in the FOXF2 gene, this test can provide definitive diagnostic information, guide treatment decisions, and offer insight into the risk of recurrence in future pregnancies.

The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. The cost includes the collection of a DNA sample, usually through a blood draw or cheek swab, the genetic analysis, and a comprehensive report detailing the findings. Patients and healthcare providers can use this information to better understand the condition, explore treatment options, and make informed decisions about care and management.

Description

FOXF2 Gene Disorders of Sex Development with Cleft Palate Genetic Test

Test Name: FOXF2 Gene Disorders of sex development with cleft palate Genetic Test

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

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: Reproductive Disorders

Doctor: Gynecology

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for FOXF2 Gene Disorders of sex development with cleft palate NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXF2 Gene Disorders of sex development with cleft palate NGS Genetic DNA Test gene FOXF2

Test Details: The FOXF2 gene is involved in the development of various tissues and organs, including the palate, which is the roof of the mouth. Mutations in this gene can lead to disorders of sex development (DSD) and cleft palate. Disorders of sex development refer to a group of conditions in which an individual’s chromosomal, gonadal, or anatomical sex is atypical. This can include conditions such as ambiguous genitalia, underdeveloped or absent reproductive organs, and other variations in sexual development. Cleft palate, on the other hand, is a congenital condition characterized by a split or opening in the roof of the mouth. It can affect feeding, speech, and overall oral health.

Next-generation sequencing (NGS) genetic tests are a type of genetic testing that can analyze multiple genes simultaneously. In the case of disorders of sex development with cleft palate, an NGS genetic test can help identify mutations or variations in the FOXF2 gene or other genes associated with these conditions. NGS genetic tests can provide valuable information for diagnosis, prognosis, and treatment planning. They can help determine the underlying cause of the disorders and guide personalized treatment options. Additionally, genetic testing can also provide information about the risk of passing on the condition to future generations. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the results.

Test Name	FOXF2 Gene Disorders of sex development with cleft palate 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	Reproductive Disorders
Doctor	Gynecology
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for FOXF2 Gene Disorders of sex development with cleft palate NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FOXF2 Gene Disorders of sex development with cleft palate NGS Genetic DNA Test gene FOXF2
Test Details	The FOXF2 gene is involved in the development of various tissues and organs, including the palate, which is the roof of the mouth. Mutations in this gene can lead to disorders of sex development (DSD) and cleft palate. Disorders of sex development refer to a group of conditions in which an individual’s chromosomal, gonadal, or anatomical sex is atypical. This can include conditions such as ambiguous genitalia, underdeveloped or absent reproductive organs, and other variations in sexual development. Cleft palate, on the other hand, is a congenital condition characterized by a split or opening in the roof of the mouth. It can affect feeding, speech, and overall oral health. Next-generation sequencing (NGS) genetic tests are a type of genetic testing that can analyze multiple genes simultaneously. In the case of disorders of sex development with cleft palate, an NGS genetic test can help identify mutations or variations in the FOXF2 gene or other genes associated with these conditions. NGS genetic tests can provide valuable information for diagnosis, prognosis, and treatment planning. They can help determine the underlying cause of the disorders and guide personalized treatment options. Additionally, genetic testing can also provide information about the risk of passing on the condition to future generations. It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate counseling and guidance based on the results.