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TYROBP Gene Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy Genetic Test Cost

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

-21%

The TYROBP gene plays a crucial role in the development of Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease. This rare, genetic disorder is characterized by bone cysts and progressive neurological deterioration. The genetic test for identifying mutations in the TYROBP gene is crucial for diagnosing PLOSL, enabling early intervention and management of the condition.

DNA Labs UAE offers this specialized genetic test to detect mutations in the TYROBP gene associated with PLOSL. The test is performed using a sample of the patient’s blood or saliva, employing advanced genetic sequencing techniques to accurately identify mutations. The cost of the test is 4400 AED, a valuable investment for individuals with a family history of the disorder or presenting symptoms of PLOSL, as it provides essential diagnostic information that can guide treatment and management decisions.

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TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy Genetic Test

Test Details

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease, is a rare genetic disorder characterized by progressive neurodegeneration and bone abnormalities. The TYROBP gene is associated with PLOSL, and mutations in this gene can cause the disease.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly and accurately sequence large amounts of DNA. It allows for the simultaneous analysis of multiple genes or even the entire exome or genome.

NGS genetic testing can be used to identify mutations in the TYROBP gene or other genes associated with PLOSL, providing a molecular diagnosis for individuals suspected of having the disease. By identifying the specific genetic mutation causing PLOSL, NGS genetic testing can help confirm the diagnosis, provide information about disease prognosis, and guide treatment decisions. It can also be used for carrier testing and prenatal testing in families with a known TYROBP gene mutation.

Test Name

TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 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

Neurological Disorders

Doctor

Neurologist

Test Department

Genetics

Pre Test Information

Clinical History of Patient who is going for TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy.

Test Name TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 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 TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TYROBP Gene Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
Test Details

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), also known as Nasu-Hakola disease, is a rare genetic disorder characterized by progressive neurodegeneration and bone abnormalities. The TYROBP gene is associated with PLOSL, and mutations in this gene can cause the disease.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to rapidly and accurately sequence large amounts of DNA. It allows for the simultaneous analysis of multiple genes or even the entire exome or genome. NGS genetic testing can be used to identify mutations in the TYROBP gene or other genes associated with PLOSL, providing a molecular diagnosis for individuals suspected of having the disease.

By identifying the specific genetic mutation causing PLOSL, NGS genetic testing can help confirm the diagnosis, provide information about disease prognosis, and guide treatment decisions. It can also be used for carrier testing and prenatal testing in families with a known TYROBP gene mutation.

SKU: TEST-1917