Chromosomal Numerical Changes: Such as duplications or deletions in specific regions of DNA, aiding in identifying genetic disorders. Congenital Defects: Can be used to detect genetic changes associated with congenital abnormalities. Genetic Diseases: Such as syndromes or conditions affecting growth and development.

Individuals with Congenital Defects: To identify potential genetic changes associated with these defects. Patients with Unexplained Symptoms: Such as delayed growth or development, or signs indicative of genetic disorders. Individuals with a Family History of Genetic Disorders: The test can be useful in assessing genetic risk. Patients with Complex Medical Conditions: Where genetic factors may contribute to the condition. Pregnant Women: Who have abnormal results in routine screenings, to evaluate the health of the fetus.

Congenital Defects: Such as physical or structural abnormalities present at birth. Delayed Growth or Development: Such as delays in speech, movement, or social skills. Unexplained Health Issues: Such as recurrent illness or unclear symptoms not explained by conventional diagnoses. Psychological or Behavioral Disorders: Such as learning difficulties or behavioral issues that may be linked to genetic factors. Family History of Genetic Disorders: Such as repeated cases of genetic diseases or congenital defects in the family.

What is the Array CGH Test? It is a genetic test used to detect copy number variations in DNA, which helps in diagnosing genetic disorders. Why is this test performed? It is conducted to identify genetic changes associated with congenital defects and genetic diseases, providing precise information about the health condition. How is the test performed? A DNA sample is usually taken from blood or tissue and then analyzed using advanced techniques. Does the patient need to fast before the test? Fasting is usually not required, but it is recommended to consult a doctor before the test. What are the normal levels that may appear? The test focuses on detecting changes and does not have specific normal levels; it depends on the presence or absence of alterations. What can affect the test results? Environmental factors, family history, and medications can influence the results. What are the risks associated with this test? The test is generally safe, but minor risks may be associated with blood collection. How can I prepare for the Array CGH test? It is recommended to discuss any medications or health conditions with your doctor before the test. When do the results appear? Results usually appear within one to three weeks, depending on the laboratory.

Focus on Genetic Changes: This test does not rely on "normal levels" like biochemical tests; it focuses on detecting DNA alterations. Negative Results: Indicate no significant genetic changes, suggesting the absence of genetic disorders in the tested sample. Positive Results: Indicate the presence of copy number changes, such as deletions or duplications in specific DNA regions, which may require further evaluation and diagnosis.

High-Res Array CGH Test | Lahalak Platform

Advanced screening to detect subtle chromosomal changes, aiding early diagnosis of genetic disorders and enabling personalized healthcare planning for a secure future.

Prices starts from: 5527.94 SAR

Scientific name: High-Resolution Array CGH Test

High-resolution array Comparative Genomic Hybridization (Array CGH) analysis is used to detect copy number variations in DNA. This advanced technique allows for highly accurate identification of genetic disorders. The test is useful in diagnosing a range of health conditions, including congenital anomalies and inherited diseases, as it helps physic...

High-Resolution Array CGH Test - Discover Your Genetic Blueprint

Service type Genetic test (Blood)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 5527.94 SAR

Included Services

Array CGH - High Resolution Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Chromosomal Numerical Changes: Such as duplications or deletions in specific regions of DNA, aiding in identifying genetic disorders.
Congenital Defects: Can be used to detect genetic changes associated with congenital abnormalities.
Genetic Diseases: Such as syndromes or conditions affecting growth and development.

Recommended groups

Individuals with Congenital Defects: To identify potential genetic changes associated with these defects.
Patients with Unexplained Symptoms: Such as delayed growth or development, or signs indicative of genetic disorders.
Individuals with a Family History of Genetic Disorders: The test can be useful in assessing genetic risk.
Patients with Complex Medical Conditions: Where genetic factors may contribute to the condition.
Pregnant Women: Who have abnormal results in routine screenings, to evaluate the health of the fetus.

Symptoms indicative

Congenital Defects: Such as physical or structural abnormalities present at birth.
Delayed Growth or Development: Such as delays in speech, movement, or social skills.
Unexplained Health Issues: Such as recurrent illness or unclear symptoms not explained by conventional diagnoses.
Psychological or Behavioral Disorders: Such as learning difficulties or behavioral issues that may be linked to genetic factors.
Family History of Genetic Disorders: Such as repeated cases of genetic diseases or congenital defects in the family.

FAQs

What is the Array CGH Test? It is a genetic test used to detect copy number variations in DNA, which helps in diagnosing genetic disorders.
Why is this test performed? It is conducted to identify genetic changes associated with congenital defects and genetic diseases, providing precise information about the health condition.
How is the test performed? A DNA sample is usually taken from blood or tissue and then analyzed using advanced techniques.
Does the patient need to fast before the test? Fasting is usually not required, but it is recommended to consult a doctor before the test.
What are the normal levels that may appear? The test focuses on detecting changes and does not have specific normal levels; it depends on the presence or absence of alterations.
What can affect the test results? Environmental factors, family history, and medications can influence the results.

Normal Levels

Focus on Genetic Changes: This test does not rely on "normal levels" like biochemical tests; it focuses on detecting DNA alterations.
Negative Results: Indicate no significant genetic changes, suggesting the absence of genetic disorders in the tested sample.
Positive Results: Indicate the presence of copy number changes, such as deletions or duplications in specific DNA regions, which may require further evaluation and diagnosis.