ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test
At DNA Labs UAE, we offer the ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test. This test is designed to detect mutations in the ACP2 gene, which can lead to lysosomal acid phosphatase deficiency, a rare genetic disorder.
Test Components
The ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test includes:
- Lysosomal acid phosphatase deficiency genetic test
Price
The cost of the ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test is 3200.0 AED.
Sample Condition
The sample required for this test is blood.
Report Delivery
You can expect to receive your test report within 3 to 4 weeks.
Method
The ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test utilizes NGS (Next Generation Sequencing) technology.
Test Type
This test falls under the category of metabolic disorders.
Doctor
This test can be ordered by a general physician.
Test Department
The ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic Test is conducted in our Genetics department.
Pre Test Information
Prior to undergoing the ACP2 Gene Lysosomal Acid Phosphatase Deficiency Genetic 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 lysosomal acid phosphatase deficiency.
Test Details
The ACP2 gene encodes for lysosomal acid phosphatase, an enzyme responsible for breaking down various molecules within the lysosomes of cells. Mutations in the ACP2 gene can result in lysosomal acid phosphatase deficiency, a rare genetic disorder.
Individuals with lysosomal acid phosphatase deficiency may experience a range of symptoms, including developmental delay, intellectual disability, seizures, skeletal abnormalities, and organ dysfunction. The severity of these symptoms can vary among affected individuals.
NGS (Next Generation Sequencing) genetic testing is utilized to analyze multiple genes or the entire genome simultaneously. This high-throughput sequencing technology allows for the rapid sequencing of large amounts of DNA. In the case of lysosomal acid phosphatase deficiency, NGS genetic testing can identify mutations or variations in the ACP2 gene, aiding in the diagnosis of the condition.
NGS genetic testing is not only used for diagnosis but also for carrier screening, prenatal testing, and predicting the risk of developing certain genetic disorders. Its implementation has revolutionized the field of genetics, enabling more comprehensive and efficient analysis of genetic material.
| Test Name | ACP2 Gene Lysosomal acid phosphatase deficiency Genetic Test |
|---|---|
| Components | |
| Price | 3200.0 AED |
| Sample Condition | Blood |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for ACP2 Gene Lysosomal acid phosphatase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Lysosomal acid phosphatase deficiency |
| Test Details | The ACP2 gene encodes for lysosomal acid phosphatase, an enzyme that plays a role in the breakdown of various molecules within the lysosomes of cells. Mutations in the ACP2 gene can lead to lysosomal acid phosphatase deficiency, which is a rare genetic disorder. Lysosomal acid phosphatase deficiency can result in a wide range of symptoms, including developmental delay, intellectual disability, seizures, skeletal abnormalities, and organ dysfunction. The severity of the symptoms can vary widely among affected individuals. NGS (Next Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. It uses high-throughput sequencing technologies to rapidly sequence large amounts of DNA. NGS can be used to identify mutations or variations in the ACP2 gene, which can help in diagnosing lysosomal acid phosphatase deficiency. NGS genetic testing can also be used for carrier screening, prenatal testing, and predicting the risk of developing certain genetic disorders. It has revolutionized the field of genetics by enabling more comprehensive and efficient analysis of genetic material. |
