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SLC25A19 Gene Microcephaly Amish Type Genetic Test Cost

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

-21%

The SLC25A19 Gene Microcephaly Amish Type Genetic Test is a specialized diagnostic tool designed to identify mutations in the SLC25A19 gene, which are linked to a rare form of microcephaly primarily found in the Amish population. Microcephaly Amish Type, also known as Amish Microcephaly, is a genetic condition characterized by significantly reduced head size and brain volume, leading to developmental delays and neurological issues. This test is crucial for early detection, allowing for appropriate intervention and support for affected individuals and their families.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab. The sample is then analyzed to detect any mutations in the SLC25A19 gene that are indicative of Microcephaly Amish Type. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology employed.

Early diagnosis through the SLC25A19 Gene Microcephaly Amish Type Genetic Test can significantly impact the management of the condition, offering insights into potential treatments and therapies. It also provides families with valuable information regarding the genetic risks for future pregnancies. DNA Labs UAE ensures confidentiality and accuracy, offering support and guidance throughout the testing process.

Description

SLC25A19 Gene Microcephaly Amish type Genetic Test

Test Name: SLC25A19 Gene Microcephaly Amish type 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 SLC25A19 Gene Microcephaly, Amish type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC25A19 Gene Microcephaly, Amish type NGS Genetic DNA Test gene SLC25A19

Test Details: The SLC25A19 gene is associated with a rare genetic disorder called microcephaly, Amish type. Microcephaly is a condition characterized by an abnormally small head size and brain development. The Amish type refers to a specific form of microcephaly that is more prevalent among the Amish population.

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

An NGS genetic test for the SLC25A19 gene would involve obtaining a DNA sample from the individual being tested, typically through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any mutations or variations in the SLC25A19 gene.

This type of genetic test can help confirm a diagnosis of microcephaly, Amish type by identifying mutations in the SLC25A19 gene. It can also be used for carrier testing to determine if an individual carries a mutation in the gene, which may be important for family planning purposes.

It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

Test Name	SLC25A19 Gene Microcephaly Amish type 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 SLC25A19 Gene Microcephaly, Amish type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC25A19 Gene Microcephaly, Amish type NGS Genetic DNA Test gene SLC25A19
Test Details	The SLC25A19 gene is associated with a rare genetic disorder called microcephaly, Amish type. Microcephaly is a condition characterized by an abnormally small head size and brain development. The Amish type refers to a specific form of microcephaly that is more prevalent among the Amish population. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. It uses high-throughput sequencing technologies to rapidly and efficiently sequence large amounts of genetic material. An NGS genetic test for the SLC25A19 gene would involve obtaining a DNA sample from the individual being tested, typically through a blood or saliva sample. The DNA is then sequenced using NGS technology to identify any mutations or variations in the SLC25A19 gene. This type of genetic test can help confirm a diagnosis of microcephaly, Amish type by identifying mutations in the SLC25A19 gene. It can also be used for carrier testing to determine if an individual carries a mutation in the gene, which may be important for family planning purposes. It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.