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LIFR Gene Stuve-Wiedemann Syndrome Genetic Test Cost

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

-21%

The LIFR Gene Stuve-Wiedemann Syndrome Genetic Test is a specialized diagnostic tool designed to detect mutations in the LIFR gene, which are responsible for causing Stuve-Wiedemann Syndrome (SWS). This rare genetic disorder is characterized by skeletal abnormalities, muscle weakness, and difficulties in regulating body temperature. Early and accurate diagnosis through genetic testing is crucial for managing the symptoms and improving the quality of life of affected individuals.

Conducted at DNA Labs UAE, this genetic test involves analyzing the patient’s DNA to identify any mutations in the LIFR gene. The process is meticulous and requires advanced technological tools to ensure accuracy. Given the complexity and the specialized nature of this test, it is priced at 4400 AED. This cost reflects the comprehensive analysis and the expertise required to interpret the results, providing families and healthcare professionals with essential information for the effective management of Stuve-Wiedemann Syndrome.

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LIFR Gene Stuve-Wiedemann Syndrome Genetic Test

At DNA Labs UAE, we offer the LIFR Gene Stuve-Wiedemann Syndrome Genetic Test at a cost of AED 4400.0. This test helps in the diagnosis of Stuve-Wiedemann Syndrome, a rare genetic disorder associated with the LIFR gene.

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

Prior to undergoing the LIFR Gene Stuve-Wiedemann Syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by the syndrome.

Test Details

The LIFR gene is associated with Stuve-Wiedemann Syndrome, a congenital condition characterized by skeletal abnormalities, respiratory difficulties, feeding problems, and a high risk of infections. Our NGS (Next-Generation Sequencing) technology allows for the simultaneous analysis of multiple genes, including the LIFR gene, to identify mutations or variations that may be causing the syndrome.

During the test, a DNA sample is obtained from the patient, typically through a blood sample or a cheek swab. This DNA is then sequenced using NGS technology to read the genetic code and identify any variations or mutations in the LIFR gene. The results of the test can confirm a diagnosis of Stuve-Wiedemann Syndrome and provide information about the specific mutation present in the LIFR gene.

Genetic testing for Stuve-Wiedemann Syndrome using NGS is particularly useful for individuals with symptoms of the disorder or a family history of the condition. It can provide a definitive diagnosis, guide treatment decisions, and offer valuable information for genetic counseling.

Test Name LIFR Gene Stuve-Wiedemann 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LIFR Gene Stuve-Wiedemann syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LIFR Gene Stuve-Wiedemann syndrome NGS Genetic DNA Test gene LIFR
Test Details

The LIFR gene is associated with a rare genetic disorder called Stuve-Wiedemann syndrome (SWS). SWS is a congenital condition characterized by skeletal abnormalities, such as bowing of the long bones, joint contractures, and a small chest cavity. It can also cause respiratory difficulties, feeding problems, and a high risk of infections.

NGS (Next-Generation Sequencing) is a genetic testing technique that allows for the simultaneous analysis of multiple genes, including the LIFR gene. This technique can identify mutations or variations in the LIFR gene that may be causing Stuve-Wiedemann syndrome. NGS can provide a comprehensive analysis of the genetic makeup of an individual, allowing for a more accurate diagnosis and potentially guiding treatment decisions.

Genetic testing for Stuve-Wiedemann syndrome using NGS involves obtaining a DNA sample from the patient, usually through a blood sample or a cheek swab. The DNA is then sequenced using NGS technology, which reads the genetic code and identifies any variations or mutations in the LIFR gene. The results of the test can help confirm a diagnosis of Stuve-Wiedemann syndrome and may also provide information about the specific mutation present in the LIFR gene.

Genetic testing for Stuve-Wiedemann syndrome using NGS can be useful for individuals who exhibit symptoms of the disorder or have a family history of the condition. It can help provide a definitive diagnosis, guide treatment decisions, and inform genetic counseling for affected individuals and their families.

SKU: TEST-4398 Category:

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