Medical Genetic Testing

We offer a range of advanced genetic tests to help diagnose conditions, assess health risks, and guide medical decisions.

Our genetic testing services include:

Karyotyping (Chromosomal Analysis)

The karyotype test examines your chromosomes to detect large changes such as extra, missing, or rearranged chromosomes. It is commonly used for diagnosing genetic syndromes, investigating infertility, and prenatal testing.

Couples with infertility can benefit from a karyotype test. Karotyping can also help to identify causes of recurrent pregnancy loss (RPL), intellectual disability, developmental delay, disorders of sex development (DSD), suspected chromosomal rearrangements, dysmorphic features, suspected chromosomal syndromes and short stature

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Together, these tests provide comprehensive insights into your genetic health.

Monogenic Disease Testing

Monogenic Disease Testing focuses on single genes to detect inherited conditions such as sickle cell anaemia and cystic fibrosis. It helps confirm diagnoses, assess risk, and support family planning.

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Panel Diagnostic Testing

Panel Diagnostic Testing analyzes multiple related genes at once to identify conditions more efficiently. It is commonly used for diseases like inherited cancers and heart conditions.

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Sequencing

Sequencing reads your DNA in detail to identify small changes in genes that may cause disease. It is widely used for diagnosing rare conditions, understanding cancer, and supporting personalized treatment.

Get Sequencing Test