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APCDD1 Gene Hypotrichosis type 1 Genetic Test Cost

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

-21%

The APCDD1 gene hypotrichosis type 1 genetic test is a specialized diagnostic tool aimed at identifying mutations in the APCDD1 gene, which are linked to hypotrichosis type 1, a rare genetic condition characterized by reduced hair growth on the scalp and body. This condition is inherited in an autosomal dominant manner, meaning a mutation in just one of the two copies of the gene can lead to the disorder. The test is crucial for confirming a diagnosis, understanding the genetic basis of the condition, and guiding treatment and management decisions.

Performed at DNA Labs UAE, a leading facility in genetic testing and analysis, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab. The laboratory then analyzes the genetic material, focusing on the APCDD1 gene to detect any mutations that are associated with hypotrichosis type 1.

The cost of the APCDD1 gene hypotrichosis type 1 genetic test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, the expertise required to accurately interpret the results, and the comprehensive service provided by the laboratory, including pre-test counseling, sample collection, genetic analysis, and post-test consultation to discuss the findings.

Description

APCDD1 Gene Hypotrichosis Type 1 Genetic Test

Test Name: APCDD1 Gene Hypotrichosis Type 1 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: Osteology Dermatology Immunology Disorders

Doctor: Dermatologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for APCDD1 Gene Hypotrichosis Type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with APCDD1 Gene Hypotrichosis Type 1 NGS Genetic DNA Test gene APCDD1.

Test Details:

APCDD1 gene hypotrichosis type 1 is a genetic disorder characterized by the loss of hair (hypotrichosis) on the scalp, eyebrows, and eyelashes. It is caused by mutations in the APCDD1 gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of mutations or changes in the DNA that may be responsible for a particular genetic disorder, such as APCDD1 gene hypotrichosis type 1. NGS genetic testing involves sequencing the entire coding region of the APCDD1 gene to identify any mutations that may be present. This can help confirm a diagnosis of APCDD1 gene hypotrichosis type 1 and provide information about the specific mutation causing the condition.

Genetic testing for APCDD1 gene hypotrichosis type 1 can be useful for individuals who have symptoms of the disorder and are seeking a diagnosis, as well as for family members who may be at risk of inheriting the condition. It can also help in genetic counseling and family planning decisions. It is important to note that genetic testing for APCDD1 gene hypotrichosis type 1 may not be available in all healthcare settings. It is recommended to consult with a healthcare professional or genetic counselor to determine the availability and appropriateness of genetic testing in specific cases.

Test Name	APCDD1 Gene Hypotrichosis type 1 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	Osteology Dermatology Immunology Disorders
Doctor	Dermatologist
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for APCDD1 Gene Hypotrichosis type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with APCDD1 Gene Hypotrichosis type 1 NGS Genetic DNA Test gene APCDD1
Test Details	APCDD1 gene hypotrichosis type 1 is a genetic disorder characterized by the loss of hair (hypotrichosis) on the scalp, eyebrows, and eyelashes. It is caused by mutations in the APCDD1 gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the detection of mutations or changes in the DNA that may be responsible for a particular genetic disorder, such as APCDD1 gene hypotrichosis type 1. NGS genetic testing involves sequencing the entire coding region of the APCDD1 gene to identify any mutations that may be present. This can help confirm a diagnosis of APCDD1 gene hypotrichosis type 1 and provide information about the specific mutation causing the condition. Genetic testing for APCDD1 gene hypotrichosis type 1 can be useful for individuals who have symptoms of the disorder and are seeking a diagnosis, as well as for family members who may be at risk of inheriting the condition. It can also help in genetic counseling and family planning decisions. It is important to note that genetic testing for APCDD1 gene hypotrichosis type 1 may not be available in all healthcare settings. It is recommended to consult with a healthcare professional or genetic counselor to determine the availability and appropriateness of genetic testing in specific cases.