Allied Healthcare Department

Hereditary Cancer Clinic

Empowering families through genetics and early prevention.

Comprehensive Allied Care. Dedicated to clinical excellence since 1954.

Our mission is to translate genetic insights into personalized prevention strategies, providing families with the knowledge to manage their cancer risk proactively.
Dr. Balaji T KAssistant Professor & In-chargeMD, Post Doctoral Fellow (IAP PHO)
Our Work

About the Department

Empowering families through genetics and early prevention.

Genetic Risk Assessment

The Hereditary Cancer Clinic focuses on identifying individuals and families at increased risk of cancer due to inherited genetic factors. While most cancers occur sporadically, approximately 8–10% are hereditary.

Genetic Counselling

Our clinic offers thorough risk assessment, genetic counselling, and tailored prevention strategies to assist patients and their families in lowering cancer risk and supporting early detection.

Clinical Care

Conditions Treated

Hereditary Breast & Ovarian Cancer (HBOC)

Lynch Syndrome

Li-Fraumeni Syndrome

Familial Adenomatous Polyposis (FAP)

Retinoblastoma

Pediatric hereditary cancers

Rare cancer predisposition syndromes

Interventions

Treatment Options

Step 1

Risk Assessment — Detailed personal and family history, pedigree analysis, and identification of high-risk individuals.

Step 2

Genetic Counseling — Pre-test counseling on benefits/limitations, informed decision-making, and psychosocial support.

Step 3

Genetic Testing — Targeted gene testing, multigene panel testing, or whole exome sequencing (by Cancer Biology and Molecular Diagnostics department).

Step 4

Personalized Risk Management — Tailored surveillance, risk-reducing strategies (medical/surgical), and lifestyle modification.

Step 5

Family-Based Care — Cascade testing for relatives and preventive strategies for family members.

When Should You Visit?

Consult our specialists if you or your loved ones experience any of the following:

Cancer diagnosis at a young age (<50 years)

Multiple primary cancers in the same individual

Family history of cancer (2 or more relatives)

Occurrence of rare cancers (e.g., male breast cancer, adrenocortical carcinoma)

Presence of a known familial genetic mutation

Bilateral tumors or multiple distinct primary sites

Get in Touch

Contact the Hereditary Cancer Clinic team

For clinical enquiries, collaborative research requests, or postgraduate academic admissions details, please contact us directly.