Molecular Precision Diagnostics for Children
Helping families worldwide find answers for rare and undiagnosed diseases: knowledge should travel, not children.
Every child deserves the chance to receive the right diagnosis and the right treatment, regardless of where they are born. Yet for many families, the search for answers stretches across years and continents, while precious time is lost. At the Dr. von Hauner Children's Hospital of LMU Munich, we have long believed that no child should suffer simply because their disease is too rare for anyone to recognise it. Our vision is rooted in a simple but powerful conviction: knowledge should travel, not children. Through scientific collaboration, shared expertise, and molecular diagnostics, we are committed to ensuring that children everywhere have access to world-class diagnostics and a future shaped not by the rarity of a disease, but by the power of science, partnership, and hope.
• Leading European pediatric center
• Rare disease expertise
• Genomic medicine and cutting-edge diagnostic platforms
• Multidisciplinary care
• Leading science in genomics, molecular sciences, AI
• Connected translational research with global partners
• Rare genetic diseases
• Inborn errors of immunity
• Neurodevelopmental disorders
• Metabolic disorders
• Hematological and bleeding disorders
• Rare pulmonary diseases
• Rare gastrointestinal and liver disorders
• Rare kidney diseases
• Endocrine diseases
• Complex syndromatic disorders
• Interdisciplinary case reviews
• Comprehensive genome sequencing (short & long read)
• Molecular diagnostics
• Research partnerships
Contact
Prof. Christoph Klein, MD PhD
Chair of Pediatrics, LMU Munich
Dr. von Hauner Childrens Hospital
Dr. Arne Pfeufer
Consultant in Human Genetics (LMU Munich & Dubai)
Dubai mobile number
E-Mail +xxxxx
Dr. Lisa Peterson
Medical Specialist in Human Genetics
Dr. von Hauner Childrens Hospital