Treatment Detail

Paediatric Genetics Services in London

A comprehensive specialist pathway for children with suspected genetic conditions, from initial clinical assessment and genetic testing through to diagnosis and coordinated long-term care.
Paediatric Genetics

What this consultation covers

Paediatric genetics is a specialised medical service that helps diagnose and manage genetic conditions in children and young people. Dr Robert Hegarty provides expert paediatric genetics consultations across London and the Southeast, offering families clear guidance and personalised care plans when standard assessments have not provided clear answers, or when specific genetic conditions are suspected.

The consultation combines detailed medical history taking, thorough physical examination, and genetic testing where appropriate to identify inherited conditions or chromosomal abnormalities. The service addresses a wide range of genetic concerns, from single gene disorders to complex chromosomal conditions, with each child’s presentation assessed individually and sensitively.

Who may benefit from this assessment

Children presenting with unexplained developmental delays, unusual growth patterns, or distinctive physical characteristics that suggest an underlying genetic cause may benefit from specialist genetics consultation. Families with a history of genetic conditions may also benefit, particularly when planning future pregnancies or when multiple family members are affected by similar symptoms.

Dr Hegarty will carefully assess whether genetic factors may be contributing to a child’s symptoms or development. Early specialist review may help establish a clear diagnosis, guide appropriate medical management, and provide families with the information they need to access targeted treatments, support services, and informed family planning decisions.

Frequently Asked Questions

How long does a genetics consultation take?

Initial genetics consultations typically last 60 to 90 minutes to allow thorough assessment and discussion of the child’s medical history, development, and family background. Follow-up appointments may be shorter, depending on the complexity of the individual case and the results of any tests arranged.

Not all children require genetic testing. Dr Hegarty will recommend testing only when it may provide useful information for diagnosis or management. All testing options are discussed thoroughly with families before any decisions are made, including the benefits, limitations, and potential implications of results.

Results timing varies depending on the type of testing required. Simple targeted tests may be available within days, while comprehensive genetic analysis or chromosomal sequencing may take several months. Families are informed of expected timescales when testing is arranged at the consultation.

Not finding a genetic cause does not mean a child’s symptoms are unimportant. The consultation may still provide valuable guidance on management and monitoring, and genetic knowledge continues to advance rapidly. Dr Hegarty will discuss all findings clearly and outline appropriate next steps regardless of the outcome.

Need advice?

Book a private consultation to discuss symptoms, test results, or ongoing concerns.

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