LMNA Gene Heart-hand syndrome Slovenian type Genetic Test
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: Dysmorphology
- Doctor: Pediatrics
- 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 a protein called lamin A/C, which plays a crucial role in maintaining the structure and function of the cell nucleus. Mutations in this gene can lead to various disorders known as laminopathies, including heart-hand syndrome, Slovenian type.
Heart-hand syndrome, Slovenian type is a rare genetic disorder characterized by abnormalities in the development of the heart and hands. Individuals with this condition typically have congenital heart defects, such as atrial septal defects or ventricular septal defects. They may also have hand anomalies, such as missing fingers or fusion of fingers.
NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. It allows for the detection of genetic variations, including mutations, deletions, or duplications, in the LMNA gene and other relevant genes associated with heart-hand syndrome, Slovenian type. This type of genetic testing can help confirm a diagnosis, provide information on disease progression, and guide treatment options.
It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate genetic counseling and guidance based on the test results.
| 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 | Dysmorphology |
| Doctor | Pediatrics |
| 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 a protein called lamin A/C, which plays a crucial role in maintaining the structure and function of the cell nucleus. Mutations in this gene can lead to various disorders known as laminopathies, including heart-hand syndrome, Slovenian type. Heart-hand syndrome, Slovenian type is a rare genetic disorder characterized by abnormalities in the development of the heart and hands. Individuals with this condition typically have congenital heart defects, such as atrial septal defects or ventricular septal defects. They may also have hand anomalies, such as missing fingers or fusion of fingers. NGS (Next-Generation Sequencing) genetic testing is a high-throughput method used to analyze multiple genes simultaneously. It allows for the detection of genetic variations, including mutations, deletions, or duplications, in the LMNA gene and other relevant genes associated with heart-hand syndrome, Slovenian type. This type of genetic testing can help confirm a diagnosis, provide information on disease progression, and guide treatment options. It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional, such as a geneticist or genetic counselor, who can provide appropriate genetic counseling and guidance based on the test results. |
