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PCNT Gene Microcephalic Osteodysplastic Primordial Dwarfism Type 2 Genetic Test Cost

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

-21%

The PCNT Gene Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD II) Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the PCNT gene, which are associated with MOPD II. This condition is characterized by extremely small stature, skeletal abnormalities, and microcephaly, where individuals have a significantly smaller head size compared to others of the same age and sex. Early detection through this genetic test can aid in the management and understanding of the condition, allowing for tailored care and support.

Priced at 4400 AED, the test involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for specific genetic alterations in the PCNT gene. The results from this test can provide crucial information for families and healthcare providers, including the confirmation of a MOPD II diagnosis, insight into the potential severity of the condition, and guidance for future family planning.

DNA Labs UAE is equipped with advanced genetic testing technology and staffed by professionals experienced in genetic diagnostics, ensuring accurate and reliable results. This test represents an important step for affected individuals and their families in understanding their condition and making informed decisions about their health and care plans.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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PCNT Gene Microcephalic Osteodysplastic Primordial Dwarfism Type 2 Genetic Test

Test Name:

PCNT Gene Microcephalic Osteodysplastic Primordial Dwarfism Type 2 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 PCNT Gene Microcephalic Osteodysplastic Primordial Dwarfism Type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PCNT Gene Microcephalic Osteodysplastic Primordial Dwarfism Type 2 NGS Genetic DNA Test gene PCNT

Test Details:

The PCNT gene is associated with a rare genetic disorder called microcephalic osteodysplastic primordial dwarfism type 2 (MOPD2). This disorder is characterized by severe growth retardation, microcephaly (small head size), skeletal abnormalities, and developmental delays. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of MOPD2, NGS genetic testing can be used to identify mutations or variations in the PCNT gene that are associated with the disorder. NGS genetic testing involves sequencing the DNA of an individual to identify specific variations in the PCNT gene. This can help in confirming a diagnosis of MOPD2 and providing information about the specific genetic mutation present in an individual. The results of NGS genetic testing can be used for various purposes, including genetic counseling, family planning, and potentially guiding treatment decisions. It is important to consult with a healthcare professional or a genetic counselor to understand the implications of the test results and to discuss any further steps or recommendations.

Test Name PCNT Gene Microcephalic osteodysplastic primordial dwarfism type 2 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 PCNT Gene Microcephalic osteodysplastic primordial dwarfism type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PCNT Gene Microcephalic osteodysplastic primordial dwarfism type 2 NGS Genetic DNA Test gene PCNT
Test Details

The PCNT gene is associated with a rare genetic disorder called microcephalic osteodysplastic primordial dwarfism type 2 (MOPD2). This disorder is characterized by severe growth retardation, microcephaly (small head size), skeletal abnormalities, and developmental delays.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of MOPD2, NGS genetic testing can be used to identify mutations or variations in the PCNT gene that are associated with the disorder.

NGS genetic testing involves sequencing the DNA of an individual to identify specific variations in the PCNT gene. This can help in confirming a diagnosis of MOPD2 and providing information about the specific genetic mutation present in an individual.

The results of NGS genetic testing can be used for various purposes, including genetic counseling, family planning, and potentially guiding treatment decisions. It is important to consult with a healthcare professional or a genetic counselor to understand the implications of the test results and to discuss any further steps or recommendations.