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MATN3 Gene Epiphyseal dysplasia multiple type 5 Genetic Test Cost

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

-21%

The MATN3 gene plays a crucial role in the development and maintenance of the skeleton, particularly in the cartilage that forms the growth regions (epiphyses) of bones. Mutations in the MATN3 gene are associated with Epiphyseal Dysplasia, Multiple, Type 5 (EDM5), a rare genetic disorder characterized by abnormalities in the developing bone and cartilage, leading to short stature, joint pain, and early-onset osteoarthritis.

To diagnose this condition, a genetic test focusing on the MATN3 gene can be conducted. This test involves analyzing the DNA to identify mutations in the MATN3 gene that are indicative of EDM5. DNA Labs UAE offers this specific genetic testing service, providing a vital tool for early diagnosis and management of the condition.

The cost of the MATN3 Gene Epiphyseal Dysplasia Multiple Type 5 Genetic Test at DNA Labs UAE is 4400 AED. This test is crucial for families with a history of the disorder, offering them a clear understanding of their genetic status and enabling healthcare providers to tailor management strategies to prevent or mitigate the symptoms associated with this condition.

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Genetic Lab Blog: MATN3 Gene Epiphyseal Dysplasia Multiple Type 5 Genetic Test

Test Name: MATN3 Gene Epiphyseal Dysplasia Multiple 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for MATN3 Gene Epiphyseal Dysplasia, Multiple, Type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MATN3 Gene Epiphyseal Dysplasia, Multiple, Type 5 NGS Genetic DNA Test gene MATN3.

Test Details:

MATN3 gene epiphyseal dysplasia, multiple, type 5 is a genetic disorder characterized by abnormalities in the growth and development of the bones in the epiphyses, which are the rounded ends of long bones. This condition is caused by mutations in the MATN3 gene, which provides instructions for producing a protein called matrilin-3. Matrilin-3 is involved in the formation and maintenance of cartilage, which is a flexible connective tissue that provides structure and support to the bones.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MATN3 gene epiphyseal dysplasia, multiple, type 5, NGS genetic testing would involve sequencing the MATN3 gene to identify any mutations or abnormalities that may be present. This can help in confirming a diagnosis and understanding the genetic basis of the condition.

NGS genetic testing can provide important information about the specific genetic changes that are responsible for a particular disorder. This information can be useful in determining the risk of recurrence in families, providing genetic counseling, and potentially guiding treatment decisions.

Test Name MATN3 Gene Epiphyseal dysplasia multiple 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for MATN3 Gene Epiphyseal dysplasia, multiple, type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with MATN3 Gene Epiphyseal dysplasia, multiple, type 5 NGS Genetic DNA Test gene MATN3
Test Details

MATN3 gene epiphyseal dysplasia, multiple, type 5 is a genetic disorder characterized by abnormalities in the growth and development of the bones in the epiphyses, which are the rounded ends of long bones. This condition is caused by mutations in the MATN3 gene, which provides instructions for producing a protein called matrilin-3. Matrilin-3 is involved in the formation and maintenance of cartilage, which is a flexible connective tissue that provides structure and support to the bones.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of MATN3 gene epiphyseal dysplasia, multiple, type 5, NGS genetic testing would involve sequencing the MATN3 gene to identify any mutations or abnormalities that may be present. This can help in confirming a diagnosis and understanding the genetic basis of the condition.

NGS genetic testing can provide important information about the specific genetic changes that are responsible for a particular disorder. This information can be useful in determining the risk of recurrence in families, providing genetic counseling, and potentially guiding treatment decisions.

SKU: TEST-2982 Category:

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