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Paediatric Genetics

The Paediatric Genetics Department at MRR Children’s Hospital provides advanced care for neonates and children affected by congenital and hereditary conditions. With expert geneticists and access to state-of-the-art genetic testing technologies, the department is a leader in early diagnosis, counselling, and personalised care planning. Our multidisciplinary team supports families through every step of the diagnostic and treatment process.

Key Features
  • Expertise in diagnosing a wide range of genetic disorders in children.
  • Comprehensive testing, including diagnostic, carrier, and prenatal screening.
  • Family-focused counselling for informed decision-making.
  • Integrated care model involving multiple paediatric subspecialties.
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Paediatric Genetics

The Paediatric Genetics Department at MRR Children’s Hospital provides advanced care for neonates and children affected by congenital and hereditary conditions. With expert geneticists and access to state-of-the-art genetic testing technologies, the department is a leader in early diagnosis, counselling, and personalised care planning. Our multidisciplinary team supports families through every step of the diagnostic and treatment process.

Key Features
  • Expertise in diagnosing a wide range of genetic disorders in children.
  • Comprehensive testing, including diagnostic, carrier, and prenatal screening.
  • Family-focused counselling for informed decision-making.
  • Integrated care model involving multiple paediatric subspecialties.
What Sets Us Apart
  • Genetic Expertise in Paediatrics: Dedicated specialists with deep experience in congenital and hereditary conditions affecting children.
  • Comprehensive Genetic Testing: Access to full-panel diagnostics, including rare disorder screening and metabolic assessments.
  • Collaborative Treatment Planning: Coordination with paediatrics, neonatology, endocrinology, and neurology for holistic care.
  • Family Support Services: Counselling that empowers families with knowledge, guidance, and psychosocial support.
Our Approach

Our Paediatric Genetics team is dedicated to:

  • Promoting early detection through advanced screening and diagnostics.
  • Developing individualised treatment and monitoring plans for affected children.
  • Guiding families with pre- and post-natal counselling for genetic risk conditions.
Sub-Services
Carrier & Prenatal Screening:
  • Identifying genetic risks in families and unborn children.
Genetic Counselling:
  • Family education, risk assessment, and reproductive planning.
Genetic Diagnostics:
  • Testing for chromosomal, metabolic, and inherited disorders.
Multispecialty Care Coordination:
  • Tailored interventions with associated medical teams.
Newborn Screening:
  • Early detection of treatable metabolic conditions.
Specialised Programmes
  • High-risk follow-up, brachial plexus care, NDT, MDT clinics.
Sports Injuries
  • Specialised care for paediatric sports-related conditions.
Bone Tumour Management
  • Surgical treatment of benign and malignant bone growths.
Why Choose Us
  • Comprehensive Services: We are among the few hospitals offering a full suite of paediatric genetic services.
  • Expert-Led Diagnostics: Our diagnostics are led by experts, with a strong focus on accuracy and early intervention.
  • Compassionate Counselling: We provide family-focused counselling that takes into account emotional and cultural aspects.
  • Advanced Facilities: We are equipped with state-of-the-art facilities and rapid reporting systems for time-sensitive decisions.
What Sets Us Apart
  • Genetic Expertise in Paediatrics: Dedicated specialists with deep experience in congenital and hereditary conditions affecting children.
  • Comprehensive Genetic Testing: Access to full-panel diagnostics, including rare disorder screening and metabolic assessments.
  • Collaborative Treatment Planning: Coordination with paediatrics, neonatology, endocrinology, and neurology for holistic care.
  • Family Support Services: Counselling that empowers families with knowledge, guidance, and psychosocial support.
Our Approach

Our Paediatric Genetics team is dedicated to:

  • Promoting early detection through advanced screening and diagnostics.
  • Developing individualised treatment and monitoring plans for affected children.
  • Guiding families with pre- and post-natal counselling for genetic risk conditions.
Sub-Services
Carrier & Prenatal Screening:
  • Identifying genetic risks in families and unborn children.
Genetic Counselling:
  • Family education, risk assessment, and reproductive planning.
Genetic Diagnostics:
  • Testing for chromosomal, metabolic, and inherited disorders.
Multispecialty Care Coordination:
  • Tailored interventions with associated medical teams.
Newborn Screening:
  • Early detection of treatable metabolic conditions.
Specialised Programmes
  • High-risk follow-up, brachial plexus care, NDT, MDT clinics.
Sports Injuries
  • Specialised care for paediatric sports-related conditions.
Bone Tumour Management
  • Surgical treatment of benign and malignant bone growths.
Why choose us
  • Comprehensive Services: We are among the few hospitals offering a full suite of paediatric genetic services.
  • Expert-Led Diagnostics: Our diagnostics are led by experts, with a strong focus on accuracy and early intervention.
  • Compassionate Counselling: We provide family-focused counselling that takes into account emotional and cultural aspects.
  • Advanced Facilities: We are equipped with state-of-the-art facilities and rapid reporting systems for time-sensitive decisions.