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SHH Gene Holoprosencephaly Type 3 Genetic Test Cost

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

-21%

The “SHH Gene Holoprosencephaly Type 3 Genetic Test” is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the SHH gene, which are linked to Type 3 Holoprosencephaly (HPE3). Holoprosencephaly is a congenital disorder characterized by the incomplete development of the brain, leading to facial deformities and neurological impairments. The SHH (Sonic Hedgehog) gene plays a crucial role in the early development of the brain and face. Mutations in this gene can disrupt normal development, resulting in the various forms of holoprosencephaly.

This genetic test is pivotal for early diagnosis, allowing for better planning and management of the condition. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for any genetic abnormalities in the SHH gene. The test is particularly recommended for families with a history of holoprosencephaly or related symptoms, providing them with crucial information regarding genetic predispositions and the risk of recurrence in future pregnancies.

The cost of the “SHH Gene Holoprosencephaly Type 3 Genetic Test” at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the specific genetic alterations associated with Type 3 Holoprosencephaly, offering invaluable insights for affected individuals and their families. Given the complexity and the specialized nature of this test, it represents a significant step forward in the field of genetic diagnostics and personalized medicine, contributing to improved outcomes and support for those dealing with this challenging condition.

Description

SHH Gene Holoprosencephaly type 3 Genetic Test

Test Name: SHH Gene Holoprosencephaly type 3 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 SHH Gene Holoprosencephaly type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SHH Gene Holoprosencephaly type 3 NGS Genetic DNA Test gene SHH

Test Details: SHH gene holoprosencephaly type 3 NGS genetic test is a genetic test that analyzes the SHH gene for mutations that are associated with holoprosencephaly type 3. Holoprosencephaly is a rare genetic disorder characterized by the incomplete development of the brain and skull in the embryo. The SHH gene, also known as Sonic Hedgehog gene, plays a crucial role in the development of the brain and face during embryonic development. Mutations in this gene can disrupt the normal development of the brain, leading to holoprosencephaly. NGS (Next-Generation Sequencing) technology is used in this genetic test to analyze the entire coding region of the SHH gene, as well as the surrounding regulatory regions, to identify any genetic variants or mutations that may be present. The SHH gene holoprosencephaly type 3 NGS genetic test is typically performed on individuals suspected to have holoprosencephaly type 3 or those with a family history of the condition. The test can help confirm a diagnosis and provide important information for genetic counseling and family planning. It is important to note that this test specifically focuses on holoprosencephaly type 3 associated with mutations in the SHH gene. There are other types of holoprosencephaly that can be caused by mutations in different genes. Therefore, this test may not be suitable for individuals suspected to have other types of holoprosencephaly. A healthcare professional or genetic counselor can provide more information and guidance regarding genetic testing options for specific cases.

Test Name	SHH Gene Holoprosencephaly type 3 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 SHH Gene Holoprosencephaly type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SHH Gene Holoprosencephaly type 3 NGS Genetic DNA Test gene SHH
Test Details	SHH gene holoprosencephaly type 3 NGS genetic test is a genetic test that analyzes the SHH gene for mutations that are associated with holoprosencephaly type 3. Holoprosencephaly is a rare genetic disorder characterized by the incomplete development of the brain and skull in the embryo. The SHH gene, also known as Sonic Hedgehog gene, plays a crucial role in the development of the brain and face during embryonic development. Mutations in this gene can disrupt the normal development of the brain, leading to holoprosencephaly. NGS (Next-Generation Sequencing) technology is used in this genetic test to analyze the entire coding region of the SHH gene, as well as the surrounding regulatory regions, to identify any genetic variants or mutations that may be present. The SHH gene holoprosencephaly type 3 NGS genetic test is typically performed on individuals suspected to have holoprosencephaly type 3 or those with a family history of the condition. The test can help confirm a diagnosis and provide important information for genetic counseling and family planning. It is important to note that this test specifically focuses on holoprosencephaly type 3 associated with mutations in the SHH gene. There are other types of holoprosencephaly that can be caused by mutations in different genes. Therefore, this test may not be suitable for individuals suspected to have other types of holoprosencephaly. A healthcare professional or genetic counselor can provide more information and guidance regarding genetic testing options for specific cases.