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ALPL Gene Hypophosphatasia Childhood Genetic Test Cost

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

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The “ALPL Gene Hypophosphatasia Childhood Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the ALPL gene, which are associated with hypophosphatasia (HPP) in children. Hypophosphatasia is a rare, inherited disorder that affects bone mineralization, leading to a range of symptoms from mild dental issues to severe skeletal abnormalities. The test specifically targets the ALPL gene, responsible for producing the enzyme alkaline phosphatase, critical for bone growth and maintenance. A mutation in this gene can result in reduced enzyme activity, leading to the symptoms associated with HPP.

This genetic test is crucial for early diagnosis and management of the condition, allowing for targeted treatment strategies to improve quality of life and prevent severe complications. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the sophisticated nature of the genetic analysis and the comprehensive insight it provides into the patient’s condition. Early diagnosis through this test can be a cornerstone in managing hypophosphatasia, offering affected children and their families hope for a better-managed condition.

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ALPL Gene Hypophosphatasia Childhood Genetic Test

Test Name: ALPL Gene Hypophosphatasia Childhood 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: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for ALPL Gene Hypophosphatasia, childhood NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Hypophosphatasia, childhood.

Test Details:

ALPL gene hypophosphatasia is a rare genetic disorder characterized by defective bone mineralization. It is caused by mutations in the ALPL gene, which provides instructions for producing an enzyme called tissue non-specific alkaline phosphatase (TNSALP). This enzyme is involved in the metabolism of minerals such as calcium and phosphate, which are essential for bone mineralization.

Children with hypophosphatasia may present with symptoms such as weak or soft bones, fractures, delayed or impaired tooth development, muscle weakness, and growth retardation. The severity of the condition can vary, with some individuals experiencing life-threatening complications.

NGS (Next-Generation Sequencing) genetic testing is a method used to identify mutations in the ALPL gene. This test involves sequencing the entire ALPL gene to detect any changes or abnormalities in the DNA sequence. NGS technology allows for the analysis of multiple genes simultaneously, making it a useful tool for diagnosing genetic disorders like hypophosphatasia.

By identifying the specific mutation in the ALPL gene, NGS genetic testing can confirm the diagnosis of hypophosphatasia and provide information about the severity and prognosis of the condition. It can also help with genetic counseling and family planning by identifying if other family members are carriers of the mutation.

It is important to note that NGS genetic testing for hypophosphatasia is typically performed in specialized genetic testing laboratories and requires a healthcare professional to order the test. The results should be interpreted by a geneticist or genetic counselor who can provide appropriate counseling and guidance based on the findings.

Test Name ALPL Gene Hypophosphatasia childhood 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ALPL Gene Hypophosphatasia, childhood NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Hypophosphatasia, childhood
Test Details

ALPL gene hypophosphatasia is a rare genetic disorder characterized by defective bone mineralization. It is caused by mutations in the ALPL gene, which provides instructions for producing an enzyme called tissue non-specific alkaline phosphatase (TNSALP). This enzyme is involved in the metabolism of minerals such as calcium and phosphate, which are essential for bone mineralization.

Children with hypophosphatasia may present with symptoms such as weak or soft bones, fractures, delayed or impaired tooth development, muscle weakness, and growth retardation. The severity of the condition can vary, with some individuals experiencing life-threatening complications.

NGS (Next-Generation Sequencing) genetic testing is a method used to identify mutations in the ALPL gene. This test involves sequencing the entire ALPL gene to detect any changes or abnormalities in the DNA sequence. NGS technology allows for the analysis of multiple genes simultaneously, making it a useful tool for diagnosing genetic disorders like hypophosphatasia.

By identifying the specific mutation in the ALPL gene, NGS genetic testing can confirm the diagnosis of hypophosphatasia and provide information about the severity and prognosis of the condition. It can also help with genetic counseling and family planning by identifying if other family members are carriers of the mutation.

It is important to note that NGS genetic testing for hypophosphatasia is typically performed in specialized genetic testing laboratories and requires a healthcare professional to order the test. The results should be interpreted by a geneticist or genetic counselor who can provide appropriate counseling and guidance based on the findings.

SKU: TEST-2477 Category:

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