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ULK2 Gene Smith-Magenis Syndrome ULK2 Related Genetic Test Cost

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

-21%

The ULK2 gene plays a crucial role in various cellular processes, including autophagy, which is the body’s way of cleaning out damaged cells to regenerate newer, healthier cells. Mutations or abnormalities in the ULK2 gene have been linked to several genetic disorders, including Smith-Magenis Syndrome (SMS), a developmental disorder characterized by distinctive facial features, behavioral problems, sleep disturbances, and intellectual disability.

To assess the risk or presence of Smith-Magenis Syndrome and related conditions, DNA Labs UAE offers a comprehensive ULK2 Related Genetic Test. This test specifically targets the ULK2 gene to identify any genetic mutations that may be associated with SMS or related disorders. The procedure involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities.

The cost of the ULK2 Related Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the collection of the sample, the genetic analysis, and the provision of a detailed report that outlines the findings. The report is an essential tool for healthcare providers, helping them to understand a patient’s genetic makeup, make accurate diagnoses, and tailor treatment plans effectively. For families and individuals, the test provides crucial insights into genetic risks, contributing to informed healthcare decisions and proactive management of potential health issues related to Smith-Magenis Syndrome and other ULK2 gene-related conditions.

Description

Genetic Lab Blog: ULK2 Gene Smith-Magenis Syndrome ULK2 Related Genetic Test Cost AED:4400.0

Test Name: ULK2 Gene Smith-Magenis Syndrome ULK2 Related Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for ULK2 Gene Smith-Magenis Syndrome ULK2 Related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ULK2 Gene Smith-Magenis Syndrome ULK2 Related.

Test Details: Gene Smith-Magenis Syndrome (SMS) is a rare genetic disorder characterized by a range of physical, cognitive, and behavioral features. It is caused by a deletion or mutation in the RAI1 gene on chromosome 17. ULK2 is a gene that has been associated with SMS, and variations in this gene may contribute to the development of the syndrome.

NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for a comprehensive analysis of the patient’s genetic information and can identify variations in genes, including ULK2, that may be associated with Smith-Magenis Syndrome.

The ULK2-related NGS Genetic Test specifically focuses on analyzing the ULK2 gene to identify any variations or mutations that may be present. This test can help in confirming a diagnosis of Smith-Magenis Syndrome and provide valuable information for genetic counseling and management of the condition.

It is important to note that the ULK2 gene is just one of many genes that can contribute to Smith-Magenis Syndrome. Therefore, a comprehensive genetic test, such as NGS, that analyzes multiple genes associated with the syndrome is recommended for an accurate diagnosis.

Test Name	ULK2 Gene Smith-Magenis syndrome ULK2 related Genetic Test
Components
Price	4400.0 AED
Sample Condition	Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery	3 to 4 Weeks
Method	NGS Technology
Test type	Neurological Disorders
Doctor	Neurologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for ULK2 Gene Smith-Magenis syndrome, ULK2 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ULK2 Gene Smith-Magenis syndrome, ULK2 related
Test Details	Gene Smith-Magenis syndrome (SMS) is a rare genetic disorder characterized by a range of physical, cognitive, and behavioral features. It is caused by a deletion or mutation in the RAI1 gene on chromosome 17. ULK2 is a gene that has been associated with SMS, and variations in this gene may contribute to the development of the syndrome. NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for a comprehensive analysis of the patient’s genetic information and can identify variations in genes, including ULK2, that may be associated with Smith-Magenis syndrome. The ULK2-related NGS Genetic Test specifically focuses on analyzing the ULK2 gene to identify any variations or mutations that may be present. This test can help in confirming a diagnosis of Smith-Magenis syndrome and provide valuable information for genetic counseling and management of the condition. It is important to note that the ULK2 gene is just one of many genes that can contribute to Smith-Magenis syndrome. Therefore, a comprehensive genetic test, such as NGS, that analyzes multiple genes associated with the syndrome is recommended for an accurate diagnosis.