General clinical genetics
Clinical genetics consultation and assessment.
GMC number: 7439887
Consultant in Clinical Genetics and Genomic Medicine
Harry Leitch is a Clinical Academic and Consultant in Clinical Genetics and Genomic Medicine at London Pregnancy Clinic through Jeen Health. He has a broad range of clinical and academic interests, with particular expertise in rare disease genetics and the interpretation of complex genomic test results.
Harry Leitch is a Clinical Academic and Consultant in Clinical Genetics and Genomic Medicine at London Pregnancy Clinic through Jeen Health. He has a broad range of clinical and academic interests, with particular expertise in rare disease genetics and the interpretation of complex genomic test results.
Harry Leitch is a Clinical Academic and Consultant in Clinical Genetics and Genomic Medicine at London Pregnancy Clinic through Jeen Health. He has a broad range of clinical and academic interests, with particular expertise in rare disease genetics and the interpretation of complex genomic test results.
Harry is passionate about supporting individuals and families through the genetic testing journey. He places strong emphasis on clear, compassionate explanations, helping patients understand the implications of results so they can make informed decisions about next steps. He provides specialist input to genetic counselling teams for complex cases and is available for individual consultations when required.
Alongside his clinical work, Harry is an active academic with a selective and up-to-date publication record. He holds a PhD from the University of Cambridge and continues to contribute to research and education in genomic medicine.
Outside medicine, Harry is a former Scottish international squash player, having represented Scotland at three Commonwealth Games, three World Team Championships, and six European Team Championships. He holds the University of Cambridge record for the most Blues in a single sport, with ten Blues in squash.
Clinical genetics consultation and assessment.
Specialist input for rare and complex genetic conditions.
Genetic screening and assessment for newborns and children.
Diagnostic assessment of dysmorphology, birth defects and developmental conditions.
Clear interpretation of complex genomic and genetic test results.
Coordinated family follow-up and cascade genetic testing.
Genetic assessment relating to infertility.
Contact us now to book an appointment — call us on 020 3687 2939.
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