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Chromosome Breakage Syndrome Test

1,800 د.إ

-25%

Chromosome Breakage Syndrome Test, offered by DNA Labs UAE, is a specialized diagnostic procedure aimed at identifying chromosomal abnormalities that predispose individuals to various genetic disorders. This test is particularly vital for detecting conditions characterized by an increased susceptibility to chromosome breakage, which can lead to cancer, developmental delays, and other severe health issues. At a cost of 1800 AED, the test involves analyzing the individual’s DNA to identify any anomalies in chromosome structure or function that could indicate the presence of a chromosome breakage syndrome, such as Fanconi anemia or Bloom syndrome. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test provides crucial insights into the genetic health of an individual, facilitating early intervention and personalized medical strategies to manage or mitigate the impact of these genetic disorders.

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Chromosome Breakage Syndrome Test

Test Details

Chromosome breakage syndrome, also known as chromosome instability syndrome, is a rare genetic disorder characterized by the inability of cells to repair DNA damage, resulting in the breakage and rearrangement of chromosomes. This condition is usually caused by mutations in genes involved in DNA repair mechanisms.

Individuals with chromosome breakage syndrome may experience a variety of symptoms, including developmental delays, growth retardation, intellectual disability, and an increased risk of cancer. They may also exhibit physical abnormalities such as facial dysmorphism, microcephaly (abnormally small head), and skeletal abnormalities.

The diagnosis of chromosome breakage syndrome is typically made based on clinical features, genetic testing, and analysis of chromosomes for structural abnormalities. Treatment options for this condition are limited and mainly focus on managing the symptoms and preventing complications. Research is ongoing to better understand the underlying mechanisms of chromosome breakage syndrome and develop potential therapies.

Genetic counseling is also important for affected individuals and their families to understand the inheritance pattern and recurrence risks associated with this condition.

Test Name: Chromosome Breakage Syndrome Test

Components:

  • Sodium Heparin Vacutainer

Price: 1800.0 AED

Sample Condition: Peripheral blood (4-5ml)

Report Delivery: 8-10 days

Method: Cell culture

Test type: Genetics

Doctor: Gynecologist

Test Department:

Pre Test Information

Chromosome Breakage Syndrome can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.

Test Details

Chromosome breakage syndrome, also known as chromosome instability syndrome, is a rare genetic disorder characterized by the inability of cells to repair DNA damage, resulting in the breakage and rearrangement of chromosomes. This condition is usually caused by mutations in genes involved in DNA repair mechanisms.

Individuals with chromosome breakage syndrome may experience a variety of symptoms, including developmental delays, growth retardation, intellectual disability, and an increased risk of cancer. They may also exhibit physical abnormalities such as facial dysmorphism, microcephaly (abnormally small head), and skeletal abnormalities.

The diagnosis of chromosome breakage syndrome is typically made based on clinical features, genetic testing, and analysis of chromosomes for structural abnormalities. Treatment options for this condition are limited and mainly focus on managing the symptoms and preventing complications. Research is ongoing to better understand the underlying mechanisms of chromosome breakage syndrome and develop potential therapies.

Genetic counseling is also important for affected individuals and their families to understand the inheritance pattern and recurrence risks associated with this condition.

Test Name Chromosome Breakage Syndrome Test
Components Sodium Heparin Vacutainer
Price 1800.0 AED
Sample Condition Peripheral blood (4-5ml)
Report Delivery 8-10 days
Method Cell culture
Test type Genetics
Doctor Gynecologist
Test Department:
Pre Test Information Chromosome Breakage Syndrome can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad.
Test Details

Chromosome breakage syndrome, also known as chromosome instability syndrome, is a rare genetic disorder characterized by the inability of cells to repair DNA damage, resulting in the breakage and rearrangement of chromosomes. This condition is usually caused by mutations in genes involved in DNA repair mechanisms.

Individuals with chromosome breakage syndrome may experience a variety of symptoms, including developmental delays, growth retardation, intellectual disability, and an increased risk of cancer. They may also exhibit physical abnormalities such as facial dysmorphism, microcephaly (abnormally small head), and skeletal abnormalities.

The diagnosis of chromosome breakage syndrome is typically made based on clinical features, genetic testing, and analysis of chromosomes for structural abnormalities. Treatment options for this condition are limited and mainly focus on managing the symptoms and preventing complications.

Research is ongoing to better understand the underlying mechanisms of chromosome breakage syndrome and develop potential therapies. Genetic counseling is also important for affected individuals and their families to understand the inheritance pattern and recurrence risks associated with this condition.