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DCX Gene LissencephalySubcortical laminal heteropia X-linked Genetic Test

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

-21%

The “DCX Gene Lissencephaly/Subcortical Band Heterotopia (SBH) X-linked Genetic Test” is a specialized diagnostic tool used to identify mutations in the DCX gene, which are linked to neurodevelopmental disorders such as Lissencephaly and Subcortical Band Heterotopia (SBH). These conditions are characterized by abnormal brain formation, leading to smooth brain surfaces (lissencephaly) or irregular bands of gray matter (SBH), which can result in severe intellectual disability, developmental delay, seizures, and motor impairment. Given the X-linked inheritance pattern, males are typically more severely affected, while females may have milder symptoms.

This genetic test, offered by DNA Labs UAE for a cost of 4400 AED, involves analyzing the patient’s DNA to detect mutations in the DCX gene that are responsible for these conditions. The test is crucial for accurate diagnosis, understanding the risk of recurrence in families, and guiding clinical management. It is performed in a state-of-the-art laboratory setting, ensuring high-quality, reliable results for affected families seeking answers and support for these challenging conditions.

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  • This test is not intended for medical diagnosis or treatment
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DCX Gene Lissencephaly/Subcortical Laminal Heteropia X-Linked Genetic Test

Introduction

DCX gene lissencephaly/subcortical laminal heterotopia, X-linked is a genetic disorder that affects brain development. It is caused by mutations in the DCX gene, which is located on the X chromosome.

Test Details

Test Name: DCX Gene Lissencephaly/Subcortical Laminal Heteropia X-Linked Genetic Test

Components: DCX gene analysis

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 DCX Gene Lissencephaly/Subcortical Laminal Heteropia, X-linked NGS Genetic DNA Test

A Genetic Counselling session to draw a pedigree chart of family members affected with DCX Gene Lissencephaly/Subcortical Laminal Heteropia, X-linked

Test Description

Next-generation sequencing (NGS) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic mutations. In the case of DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, NGS genetic testing can be used to detect mutations in the DCX gene.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the identification of genetic variations and mutations that may be associated with the disorder.

Benefits of the Test

By performing NGS genetic testing for DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, healthcare professionals can diagnose the condition and provide appropriate genetic counseling and management options for affected individuals and their families.

Test Name DCX Gene LissencephalySubcortical laminal heteropia X-linked 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 DCX Gene Lissencephaly/Subcortical laminal heteropia, X-linked NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DCX Gene Lissencephaly/Subcortical laminal heteropia, X-linked
Test Details

DCX gene lissencephaly/subcortical laminal heterotopia, X-linked is a genetic disorder that affects brain development. It is caused by mutations in the DCX gene, which is located on the X chromosome.

Next-generation sequencing (NGS) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic mutations. In the case of DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, NGS genetic testing can be used to detect mutations in the DCX gene.

NGS genetic testing involves sequencing the DNA of an individual and comparing it to a reference genome. This allows for the identification of genetic variations and mutations that may be associated with the disorder.

By performing NGS genetic testing for DCX gene lissencephaly/subcortical laminal heterotopia, X-linked, healthcare professionals can diagnose the condition and provide appropriate genetic counseling and management options for affected individuals and their families.