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KRT14 Gene Naegeli-Franceschetti-Jadassohn Syndrome Genetic Test Cost

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

-21%

The KRT14 Gene Naegeli-Franceschetti-Jadassohn (NFJ) Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the KRT14 gene, which are responsible for the rare genetic disorder known as Naegeli-Franceschetti-Jadassohn Syndrome. This condition is characterized by a range of dermatological manifestations including reticular skin pigmentation, palmoplantar keratoderma, and in some cases, dental anomalies and diminished sweating (hypohidrosis). The test plays a crucial role in confirming the diagnosis, allowing for appropriate management and genetic counseling for affected individuals and their families. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results. By opting for this test at DNA Labs UAE, patients and healthcare providers can expect reliable and accurate genetic insights, paving the way for better understanding and management of Naegeli-Franceschetti-Jadassohn Syndrome.

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KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome Genetic Test

Cost: AED 4400.0

Symptoms, Diagnosis, and Test Details

The KRT14 gene is responsible for encoding the keratin 14 protein, which is a structural protein found in the skin, hair, and nails. Mutations in this gene can cause Naegeli-Franceschetti-Jadassohn syndrome (NFJS), a rare genetic disorder characterized by abnormal skin pigmentation, thickening of the skin on the palms and soles, and the absence or reduction of sweat glands.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of NFJS, NGS can be used to identify mutations in the KRT14 gene or other genes associated with the syndrome. This type of testing can provide a comprehensive analysis of an individual’s genetic makeup and help diagnose the underlying cause of their symptoms.

By identifying the specific genetic mutation causing NFJS, NGS genetic testing can also be used for carrier screening and prenatal diagnosis in families with a history of the condition. Additionally, it can aid in genetic counseling and management of the disorder.

Test Components and Price

Components: KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome Genetic Test

Price: AED 4400.0

Sample Condition

Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery

3 to 4 Weeks

Method

NGS Technology

Test Type

Osteology Dermatology Immunology Disorders

Doctor

Dermatologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome NGS Genetic DNA Test gene KRT14.

Test Name KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with KRT14 Gene Naegeli-Franceschetti-Jadassohn syndrome NGS Genetic DNA Test gene KRT14
Test Details

The KRT14 gene is responsible for encoding the keratin 14 protein, which is a structural protein found in the skin, hair, and nails. Mutations in this gene can cause Naegeli-Franceschetti-Jadassohn syndrome (NFJS), which is a rare genetic disorder characterized by abnormal skin pigmentation, thickening of the skin on the palms and soles, and the absence or reduction of sweat glands.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of NFJS, NGS can be used to identify mutations in the KRT14 gene or other genes associated with the syndrome. This type of testing can provide a comprehensive analysis of an individual’s genetic makeup and help diagnose the underlying cause of their symptoms.

By identifying the specific genetic mutation causing NFJS, NGS genetic testing can also be used for carrier screening and prenatal diagnosis in families with a history of the condition. Additionally, it can aid in genetic counseling and management of the disorder.