PQBP1 Gene Renpenning Syndrome Genetic Test sale cost 4400 AED
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PQBP1 Gene Renpenning Syndrome Genetic Test Cost

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

-21%

The PQBP1 Gene Renpenning Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PQBP1 gene, which are linked to Renpenning syndrome. Renpenning syndrome is a rare X-linked intellectual disability disorder that primarily affects males, characterized by developmental delays, microcephaly, short stature, and in some cases, physical deformities. The test, which costs 4400 AED, involves analyzing the patient’s DNA to detect any genetic abnormalities in the PQBP1 gene, providing crucial information for accurate diagnosis and potential management plans for affected individuals and their families. This genetic test is a significant tool for clinicians and genetic counselors in understanding the genetic basis of the syndrome, facilitating early intervention and support for those diagnosed with this condition.

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PQBP1 Gene Renpenning syndrome Genetic Test

Components: PQBP1 Gene Renpenning syndrome Genetic Test

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 PQBP1 Gene Renpenning syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PQBP1 Gene Renpenning syndrome.

Test Details: The PQBP1 gene is associated with Renpenning syndrome, which is a rare genetic disorder characterized by intellectual disability, speech and language impairments, and certain physical features. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Renpenning syndrome, NGS genetic testing can be used to identify mutations or variations in the PQBP1 gene that may be responsible for the disorder. NGS genetic testing for Renpenning syndrome involves obtaining a DNA sample from the individual being tested, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to analyze the entire coding region of the PQBP1 gene. The results of the NGS genetic test can provide information about any mutations or variations in the PQBP1 gene that may be present in the individual being tested. This information can help confirm a diagnosis of Renpenning syndrome and provide valuable information for genetic counseling and family planning.

Test Name PQBP1 Gene Renpenning syndrome 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 PQBP1 Gene Renpenning syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with PQBP1 Gene Renpenning syndrome
Test Details

The PQBP1 gene is associated with Renpenning syndrome, which is a rare genetic disorder characterized by intellectual disability, speech and language impairments, and certain physical features.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of Renpenning syndrome, NGS genetic testing can be used to identify mutations or variations in the PQBP1 gene that may be responsible for the disorder.

NGS genetic testing for Renpenning syndrome involves obtaining a DNA sample from the individual being tested, usually through a blood sample or cheek swab. The DNA is then sequenced using NGS technology to analyze the entire coding region of the PQBP1 gene.

The results of the NGS genetic test can provide information about any mutations or variations in the PQBP1 gene that may be present in the individual being tested. This information can help confirm a diagnosis of Renpenning syndrome and provide valuable information for genetic counseling and family planning.

SKU: TEST-1955 Category:

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