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TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test

4,400 د.إ

-21%

The TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the TMCO1 gene. These mutations are associated with a rare genetic disorder characterized by distinct facial features, abnormalities in skeletal development, and intellectual disability. The syndrome represents a complex condition that requires precise genetic analysis for accurate diagnosis and management.

The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic alterations in the TMCO1 gene. This gene plays a crucial role in various developmental processes, and its mutation can lead to the syndrome’s characteristic symptoms.

DNA Labs UAE offers this comprehensive genetic test for individuals showing symptoms of the syndrome or for those with a family history of genetic disorders. The cost of the test is set at 4400 AED, reflecting the intricate processes and sophisticated technology employed in identifying the genetic mutations associated with this condition. The results from this test can provide essential information for families and healthcare providers, guiding potential treatment options and management strategies for affected individuals.

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TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test

Test Name: TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test

Components: TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test

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: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome

Test Details: The TMCO1 gene is associated with a rare genetic disorder known as Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome. This syndrome is characterized by a range of physical and developmental abnormalities, including distinctive facial features, skeletal abnormalities, intellectual disability, and delayed development of motor skills. NGS genetic testing can be used to identify mutations in the TMCO1 gene that may be responsible for this syndrome. This type of testing involves sequencing the entire coding region of the gene to identify any changes or mutations that may be present. Identification of TMCO1 gene mutations can provide valuable information for families affected by this syndrome, including information about inheritance patterns, recurrence risks, and potential treatment options. It can also help clinicians better understand the underlying mechanisms of the disorder and develop more targeted therapies in the future.

Test Name TMCO1 Gene Craniofacial dysmorphism skeletal anomalies and mental retardation syndrome Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TMCO1 Gene Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TMCO1 Gene Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
Test Details

The TMCO1 gene is associated with a rare genetic disorder known as Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome. This syndrome is characterized by a range of physical and developmental abnormalities, including distinctive facial features, skeletal abnormalities, intellectual disability, and delayed development of motor skills.

NGS genetic testing can be used to identify mutations in the TMCO1 gene that may be responsible for this syndrome. This type of testing involves sequencing the entire coding region of the gene to identify any changes or mutations that may be present.

Identification of TMCO1 gene mutations can provide valuable information for families affected by this syndrome, including information about inheritance patterns, recurrence risks, and potential treatment options. It can also help clinicians better understand the underlying mechanisms of the disorder and develop more targeted therapies in the future.