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Paternal UPD Chr. 14 Gene Kagami-Ogata Syndrome Genetic Test Cost

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

-21%

Paternal Uniparental Disomy (UPD) of Chromosome 14, also known as Kagami-Ogata Syndrome, is a rare genetic condition that occurs when a child inherits two copies of chromosome 14 from their father, instead of one copy from each parent. This results in a range of developmental issues and physical abnormalities, including distinctive facial features, skeletal anomalies, and growth retardation.

The genetic test for Kagami-Ogata Syndrome involves analyzing the patient’s DNA to detect the presence of paternal UPD on chromosome 14. This test is crucial for the accurate diagnosis and management of the syndrome, allowing for early intervention and support for affected individuals and their families.

In the UAE, this specialized genetic test can be conducted at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the test is 4400 AED, which covers the comprehensive analysis required to detect this specific uniparental disomy. Given the complexity and rarity of Kagami-Ogata Syndrome, accessing this test can provide essential insights for affected families, guiding treatment and support options.

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Paternal UPD chr. 14 Gene Kagami-Ogata Syndrome Genetic Test

Test Name: Paternal UPD chr. 14 Gene Kagami-Ogata Syndrome Genetic Test

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

Price: 4400.0 AED

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 paternal UPD chr. 14 Gene Kagami-Ogata Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with paternal UPD chr. 14 Gene Kagami-Ogata Syndrome NGS Genetic DNA Test gene paternal UPD chr. 14

Test Details

Paternal UPD (Uniparental Disomy) refers to a situation where an individual inherits both copies of a chromosome pair from one parent, instead of one copy from each parent. In the context of chromosome 14, paternal UPD chr. 14 refers to the inheritance of two copies of chromosome 14 from the father, instead of one copy from the father and one copy from the mother.

Gene Kagami-Ogata Syndrome is a rare genetic disorder associated with paternal UPD chr. 14. It is characterized by overgrowth, developmental delay, intellectual disability, and distinct facial features. Individuals with this syndrome may also have other health issues such as hypotonia (low muscle tone), scoliosis (abnormal curvature of the spine), and heart defects.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It can provide a comprehensive analysis of an individual’s genetic makeup and identify any mutations or variations that may be associated with certain genetic disorders, including Gene Kagami-Ogata Syndrome.

The NGS Genetic Test for Gene Kagami-Ogata Syndrome would involve sequencing the relevant genes associated with the syndrome, such as those on chromosome 14. This test can help confirm a diagnosis and provide important information for medical management and genetic counseling.

Test Name paternal UPD chr. 14 Gene Kagami-Ogata syndrome 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 paternal UPD chr. 14 Gene Kagami-Ogata syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with paternal UPD chr. 14 Gene Kagami-Ogata syndrome NGS Genetic DNA Test gene paternal UPD chr. 14
Test Details

Paternal UPD (Uniparental Disomy) refers to a situation where an individual inherits both copies of a chromosome pair from one parent, instead of one copy from each parent. In the context of chromosome 14, paternal UPD chr. 14 refers to the inheritance of two copies of chromosome 14 from the father, instead of one copy from the father and one copy from the mother.

Gene Kagami-Ogata syndrome is a rare genetic disorder associated with paternal UPD chr. 14. It is characterized by overgrowth, developmental delay, intellectual disability, and distinct facial features. Individuals with this syndrome may also have other health issues such as hypotonia (low muscle tone), scoliosis (abnormal curvature of the spine), and heart defects.

NGS (Next-Generation Sequencing) Genetic Test refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It can provide a comprehensive analysis of an individual’s genetic makeup and identify any mutations or variations that may be associated with certain genetic disorders, including Gene Kagami-Ogata syndrome.

The NGS Genetic Test for Gene Kagami-Ogata syndrome would involve sequencing the relevant genes associated with the syndrome, such as those on chromosome 14. This test can help confirm a diagnosis and provide important information for medical management and genetic counseling.

SKU: TEST-4184 Category:

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