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LMNA Gene Heart-hand syndrome Slovenian type Genetic Test

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

-21%

The LMNA Gene Heart-hand syndrome Slovenian type genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the LMNA gene associated with Heart-hand syndrome, Slovenian type. This condition is a rare genetic disorder characterized by a combination of heart disease, particularly cardiomyopathy or arrhythmias, and deformities in the hands and upper extremities. The LMNA gene plays a crucial role in the structure and function of cells in the body, and mutations in this gene can lead to a variety of health issues, including those affecting the heart and limbs.

Given the rarity and specific genetic basis of this syndrome, the test is vital for accurate diagnosis, enabling targeted management and treatment strategies for affected individuals. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any mutations in the LMNA gene that are indicative of Heart-hand syndrome, Slovenian type.

DNA Labs UAE offers this comprehensive genetic test for a cost of 4400 AED. The facility is equipped with state-of-the-art technology and staffed by experts in genetics and molecular biology, ensuring high accuracy and reliability of the test results. Individuals who have a family history of Heart-hand syndrome, Slovenian type, or exhibit symptoms related to the condition are candidates for this test. Early diagnosis through genetic testing can significantly improve the management of the syndrome, allowing for timely interventions and a better understanding of the condition’s progression and implications.

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LMNA Gene Heart-hand syndrome Slovenian type Genetic Test

Welcome to DNA Labs UAE, where we offer the LMNA Gene Heart-hand syndrome Slovenian type Genetic Test. This test can help diagnose individuals with heart-hand syndrome, Slovenian type, a rare genetic disorder characterized by abnormalities in both the heart and the hands.

Test Components

The LMNA Gene Heart-hand syndrome Slovenian type Genetic Test includes:

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Cardiovascular Pneumology Disorders
  • Doctor: Cardiologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the LMNA Gene Heart-hand syndrome Slovenian type Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic DNA Test.

Test Details

The LMNA gene is responsible for encoding the lamin A/C protein, which plays a crucial role in maintaining the structural integrity of the cell nucleus. Mutations in the LMNA gene can lead to a group of disorders known as laminopathies, including heart-hand syndrome, Slovenian type.

Heart-hand syndrome, Slovenian type is characterized by congenital heart defects, such as atrial septal defects or ventricular septal defects, as well as hand abnormalities like syndactyly (fusion of fingers) or brachydactyly (shortened fingers).

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously. This type of genetic testing can identify mutations or variations in the LMNA gene associated with heart-hand syndrome, Slovenian type. To conduct the test, a DNA sample is obtained from the patient, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the LMNA gene.

The results of the genetic test can confirm a diagnosis of heart-hand syndrome, Slovenian type and provide valuable information for genetic counseling and management of the condition. It is important to note that genetic testing should be performed by a qualified healthcare professional, such as a geneticist or genetic counselor, who can interpret the results and provide appropriate guidance and support.

Test Name LMNA Gene Heart-hand syndrome Slovenian 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 Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with LMNA Gene Heart-hand syndrome, Slovenian type NGS Genetic DNA Test gene LMNA
Test Details

The LMNA gene is responsible for encoding the lamin A/C protein, which plays a crucial role in maintaining the structural integrity of the cell nucleus. Mutations in the LMNA gene can lead to a group of disorders known as laminopathies, which include heart-hand syndrome, Slovenian type.

Heart-hand syndrome, Slovenian type is a rare genetic disorder characterized by abnormalities in both the heart and the hands. Individuals with this condition typically have congenital heart defects, such as atrial septal defects or ventricular septal defects, as well as hand abnormalities, such as syndactyly (fusion of fingers) or brachydactyly (shortened fingers).

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes. This type of genetic testing can be used to identify mutations or variations in the LMNA gene associated with heart-hand syndrome, Slovenian type.

NGS genetic testing involves obtaining a DNA sample from the patient, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to identify any mutations or variations in the LMNA gene. The results of the genetic test can help confirm a diagnosis of heart-hand syndrome, Slovenian type and provide valuable information for genetic counseling and management of the condition.

It is important to note that genetic testing should be conducted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can interpret the results and provide appropriate guidance and support.