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IGF1 Gene Growth Retardation with Deafness and Mental Retardation Due to IGF1 Deficiency Genetic Test Cost

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

-21%

The “IGF1 Gene Growth Retardation with Deafness and Mental Retardation Due to IGF1 Deficiency Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the IGF1 gene. These mutations can lead to a rare disorder characterized by growth retardation, deafness, and mental retardation, stemming from a deficiency in the Insulin-like Growth Factor 1 (IGF1). IGF1 plays a crucial role in childhood growth and continues to have anabolic effects in adults. A deficiency in this protein can, therefore, lead to various developmental issues.

The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for any genetic abnormalities in the IGF1 gene. This testing is crucial for early diagnosis and management of the condition, allowing for tailored treatment plans that can significantly improve the quality of life for affected individuals.

The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the profound impact its results can have on the management of the condition. Conducted at DNA Labs UAE, this test represents a vital resource for families seeking answers to complex growth and developmental issues related to IGF1 deficiency.

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IGF1 Gene Growth Retardation with Deafness and Mental Retardation Genetic Test

At DNA Labs UAE, we offer the IGF1 Gene Growth Retardation with Deafness and Mental Retardation Genetic Test. This test is designed to diagnose individuals who may be experiencing growth retardation, deafness, and mental retardation due to IGF1 deficiency. By analyzing the IGF1 gene using NGS technology, we can identify any mutations or variations that may be causing the condition.

Test Components and Price

The IGF1 Gene Growth Retardation with Deafness and Mental Retardation Genetic Test is priced at 4400.0 AED. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card. The report will be delivered within 3 to 4 weeks.

Symptoms and Diagnosis

Individuals with IGF1 deficiency may experience symptoms such as growth retardation, deafness, and mental retardation. To diagnose this condition, it is important to provide the clinical history of the patient. A genetic counseling session may also be conducted to draw a pedigree chart of family members affected by IGF1 deficiency.

NGS Technology and Test Type

NGS technology, also known as Next-Generation Sequencing, is used to analyze multiple genes simultaneously. In the case of IGF1 deficiency, NGS genetic testing can identify any mutations or variations in the IGF1 gene. This method allows for a comprehensive analysis that can aid in diagnosis, prognosis, and treatment options.

Doctor and Test Department

The IGF1 Gene Growth Retardation with Deafness and Mental Retardation Genetic Test is conducted by our experienced pediatric geneticists. The test falls under the Genetics department.

Pre Test Information

Before undergoing the IGF1 Gene Growth Retardation with Deafness and Mental Retardation Genetic Test, it is important to provide the clinical history of the patient. This information will help in interpreting the test results accurately. Additionally, a genetic counseling session may be conducted to gather information about family members affected by IGF1 deficiency.

Importance of Genetic Testing

Genetic testing is crucial in identifying the specific genetic alterations causing IGF1 deficiency. It can assist in diagnosis, prognosis, and potentially guide treatment options. Additionally, genetic testing can provide valuable information for genetic counseling and family planning, allowing individuals to determine the risk of passing on the condition to future generations.

It is important to note that genetic testing should be performed and interpreted by qualified geneticists or genetic counselors. They can provide detailed information about the specific genetic variant and its implications. It is also best to consult with a healthcare professional to determine the most appropriate course of action, as genetic testing may not be available or necessary in all cases.

Test Name IGF1 Gene Growth retardation with deafness and mental retardation due to IGF1 deficiency 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 IGF1 Gene Growth retardation with deafness and mental retardation due to IGF1 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with IGF1 Gene Growth retardation with deafness and mental retardation due to IGF1 deficiency NGS Genetic DNA Test gene IGF1
Test Details

The IGF1 gene is responsible for producing insulin-like growth factor 1, which plays a crucial role in growth and development. Mutations or deficiencies in this gene can lead to various disorders, including growth retardation, deafness, and mental retardation.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations. In the case of IGF1 deficiency, NGS genetic testing can be used to identify any mutations or variations in the IGF1 gene that may be causing the condition.

By identifying the specific genetic alteration causing IGF1 deficiency, NGS genetic testing can help with diagnosis, prognosis, and potentially guide treatment options. It can also help in genetic counseling and family planning by determining the risk of passing on the condition to future generations.

It is important to note that genetic testing should be performed and interpreted by a qualified geneticist or genetic counselor, as they can provide detailed information about the specific genetic variant and its implications. Additionally, genetic testing may not be available or necessary in all cases, so it is best to consult with a healthcare professional to determine the most appropriate course of action.