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Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test Cost

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

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The “Maternal UPD Chr. 14 Gene Temple Syndrome Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to detect Temple Syndrome resulting from maternal uniparental disomy of chromosome 14 (UPD(14)mat). Temple Syndrome is a rare genetic disorder characterized by a range of symptoms including developmental delays, muscle weakness, feeding difficulties, and distinctive facial features. This condition is caused when a child inherits two copies of chromosome 14 from their mother and none from their father, leading to an imbalance in gene expression.

The test involves a comprehensive analysis of the genetic material to identify the specific chromosomal anomaly associated with Temple Syndrome. It is crucial for early diagnosis and management of the condition, allowing healthcare providers to offer targeted interventions and support to affected individuals and their families.

DNA Labs UAE offers this genetic test at a cost of 4400 AED. The lab is equipped with state-of-the-art technology and staffed by experienced professionals, ensuring accurate and reliable results. Families seeking answers about developmental concerns or individuals with a family history of Temple Syndrome may find this test particularly beneficial. It represents a crucial step towards understanding and managing the condition, offering hope and guidance for affected individuals.

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Maternal UPD chr. 14 Gene Temple Syndrome Genetic Test

Introduction

Maternal UPD (Uniparental Disomy) chr. 14 refers to a genetic condition where an individual inherits both copies of chromosome 14 from their mother, instead of one copy from each parent. This occurs when there is an error in the process of chromosome segregation during egg formation.

Maternal UPD chr. 14 can result in a variety of symptoms and health issues, including developmental delays, intellectual disability, growth abnormalities, and distinctive facial features. Gene Temple syndrome is a term that is sometimes used to describe the combination of maternal UPD chr. 14 and Temple syndrome.

Temple syndrome, also known as 14q32 imprinting center defect, is a rare genetic disorder caused by abnormalities in the region of chromosome 14 known as the 14q32 imprinted region. It is characterized by growth restriction, early puberty, and a specific pattern of facial features.

Test Details

The maternal UPD chr. 14 Gene Temple Syndrome Genetic Test offered by DNA Labs UAE utilizes NGS (Next-Generation Sequencing) Technology. This advanced sequencing technology allows for the analysis of an individual’s DNA to detect various genetic mutations, including those associated with maternal UPD chr. 14 and Temple syndrome.

Test Name: Maternal UPD chr. 14 Gene Temple Syndrome Genetic Test

  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient who is going for maternal UPD chr. 14 Gene Temple Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with maternal UPD chr. 14 Gene Temple Syndrome NGS Genetic DNA Test gene maternal UPD chr. 14

Conclusion

The maternal UPD chr. 14 Gene Temple Syndrome Genetic Test is an important tool for diagnosing and managing maternal UPD chr. 14 and Temple syndrome. By utilizing NGS Technology, DNA Labs UAE can provide accurate and detailed genetic testing services to help individuals and their families understand and manage these genetic conditions.

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

Maternal UPD (Uniparental Disomy) chr. 14 refers to a genetic condition where an individual inherits both copies of chromosome 14 from their mother, instead of one copy from each parent. This occurs when there is an error in the process of chromosome segregation during egg formation. Maternal UPD chr. 14 can result in a variety of symptoms and health issues, including developmental delays, intellectual disability, growth abnormalities, and distinctive facial features.

Gene Temple syndrome is a term that is sometimes used to describe the combination of maternal UPD chr. 14 and Temple syndrome. Temple syndrome, also known as 14q32 imprinting center defect, is a rare genetic disorder caused by abnormalities in the region of chromosome 14 known as the 14q32 imprinted region. It is characterized by growth restriction, early puberty, and a specific pattern of facial features.

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technology to analyze an individual’s DNA. NGS can be used to detect various genetic mutations, including those associated with maternal UPD chr. 14 and Temple syndrome. This type of genetic testing can help diagnose these conditions, determine the underlying genetic cause, and provide information for medical management and genetic counseling.

SKU: TEST-4404 Category:

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