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LBR Gene Pelger-Huet Anomaly Genetic Test Cost

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

-21%

The LBR Gene Pelger-Huët Anomaly Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the LBR gene, which are responsible for Pelger-Huët anomaly (PHA). This genetic condition is characterized by abnormal nuclear shape and segmentation in granulocytes, a type of white blood cell, leading to a distinctive hypolobulated appearance. These cellular abnormalities, while often benign and asymptomatic, can sometimes be indicative of more severe bone disorders or be confused with more serious hematological diseases.

DNA Labs UAE offers this precise genetic test as a part of its comprehensive portfolio, utilizing advanced genetic sequencing technologies to accurately detect the presence of mutations in the LBR gene. The test is crucial for individuals with a family history of PHA or those who exhibit hematological findings suggestive of this anomaly, as it aids in confirming the diagnosis, understanding the condition’s severity, and guiding potential treatment options.

The cost of the LBR Gene Pelger-Huët Anomaly Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the meticulous process of DNA analysis, ensuring that individuals receive accurate and reliable results. Given the specialized nature of this test, it represents a critical step for affected individuals or families in managing and understanding their genetic health landscape.

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LBR Gene Pelger-Huet Anomaly Genetic Test

At DNA Labs UAE, we offer the LBR Gene Pelger-Huet anomaly Genetic Test to help diagnose and understand the genetic basis of Pelger-Huet anomaly (PHA). This test analyzes the LBR gene for mutations associated with PHA, a rare inherited disorder characterized by abnormal shape and structure of the nucleus in white blood cells.

Test Details

  • Test Name: LBR Gene Pelger-Huet anomaly Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the LBR Gene Pelger-Huet anomaly NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with LBR Gene Pelger-Huet anomaly NGS Genetic DNA Test gene LBR.

Test Method

The LBR Gene Pelger-Huet anomaly NGS Genetic Test utilizes next-generation sequencing (NGS) technology to examine the LBR gene. This gene provides instructions for producing a protein called lamin B receptor. Mutations in the LBR gene can lead to the development of PHA. NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of genetic variations that may contribute to PHA.

Test Benefits

The LBR Gene Pelger-Huet anomaly NGS Genetic Test can identify specific mutations in the LBR gene, helping to confirm a diagnosis of PHA. It also provides valuable information for genetic counseling and management of the condition. With this test, healthcare professionals can better understand the genetic basis of Pelger-Huet anomaly and provide appropriate care and support to patients.

Overall, the LBR Gene Pelger-Huet anomaly NGS Genetic Test offered by DNA Labs UAE is a useful tool in diagnosing and understanding PHA. It is recommended for individuals with symptoms or a family history of PHA.

Test Name LBR Gene Pelger-Huet anomaly 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 LBR Gene Pelger-Huet anomaly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LBR Gene Pelger-Huet anomaly NGS Genetic DNA Test gene LBR
Test Details

The LBR Gene Pelger-Huet anomaly NGS Genetic Test is a genetic test that analyzes the LBR gene for mutations associated with Pelger-Huet anomaly (PHA). PHA is a rare inherited disorder characterized by abnormal shape and structure of the nucleus in white blood cells.

The test uses next-generation sequencing (NGS) technology to examine the LBR gene, which provides instructions for producing a protein called lamin B receptor. Mutations in this gene can lead to the development of PHA.

NGS technology allows for the simultaneous analysis of multiple genes, providing a comprehensive evaluation of genetic variations that may contribute to PHA. The test can identify specific mutations in the LBR gene, helping to confirm a diagnosis of PHA and providing valuable information for genetic counseling and management of the condition.

Overall, the LBR Gene Pelger-Huet anomaly NGS Genetic Test is a useful tool in diagnosing and understanding the genetic basis of Pelger-Huet anomaly.

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