Sale!

ASPM Gene Microcephaly Autosomal Recessive Type 5 Genetic Test Cost

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

-21%

The “ASPM Gene Microcephaly Autosomal Recessive Type 5 Genetic Test” is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the ASPM gene, which are linked to Microcephaly Autosomal Recessive Type 5. This condition is characterized by a significantly smaller head size compared to others of the same age and sex, and it can lead to developmental delays and neurological issues. The test aims to provide crucial genetic information that can aid in the diagnosis, management, and understanding of the condition. The cost of the test is 4400 AED, making it a valuable option for those seeking detailed insights into specific genetic factors contributing to microcephaly in affected individuals. By identifying mutations in the ASPM gene, healthcare providers can offer more targeted support and interventions for patients and their families.

Description

ASPM Gene Microcephaly Autosomal Recessive Type 5 Genetic Test

Test Name: ASPM Gene Microcephaly Autosomal Recessive Type 5 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 ASPM Gene Microcephaly, Autosomal Recessive Type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ASPM Gene Microcephaly, Autosomal Recessive Type 5 NGS Genetic DNA Test gene ASPM

Test Details: ASPM gene microcephaly, autosomal recessive type 5 is a genetic disorder characterized by the development of a smaller than average head size (microcephaly) and intellectual disability. It is caused by mutations in the ASPM gene, which is involved in brain development. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of ASPM gene microcephaly, autosomal recessive type 5, NGS genetic testing can be used to identify mutations in the ASPM gene that are responsible for the disorder. This type of genetic testing can help diagnose individuals with microcephaly and determine the specific genetic cause of their condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families at risk of having a child with microcephaly. NGS genetic testing is a powerful tool for identifying genetic mutations and can provide valuable information for individuals and families affected by ASPM gene microcephaly, autosomal recessive type 5. It can aid in genetic counseling, family planning, and potentially guide treatment options or interventions.

Test Name	ASPM Gene Microcephaly autosomal recessive type 5 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 ASPM Gene Microcephaly, autosomal recessive type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ASPM Gene Microcephaly, autosomal recessive type 5 NGS Genetic DNA Test gene ASPM
Test Details	ASPM gene microcephaly, autosomal recessive type 5 is a genetic disorder characterized by the development of a smaller than average head size (microcephaly) and intellectual disability. It is caused by mutations in the ASPM gene, which is involved in brain development. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of ASPM gene microcephaly, autosomal recessive type 5, NGS genetic testing can be used to identify mutations in the ASPM gene that are responsible for the disorder. This type of genetic testing can help diagnose individuals with microcephaly and determine the specific genetic cause of their condition. It can also be used for carrier testing in individuals with a family history of the disorder or for prenatal testing in families at risk of having a child with microcephaly. NGS genetic testing is a powerful tool for identifying genetic mutations and can provide valuable information for individuals and families affected by ASPM gene microcephaly, autosomal recessive type 5. It can aid in genetic counseling, family planning, and potentially guide treatment options or interventions.