Neonatal Marfan syndrome is a rare, severe and life-threatening genetic disease, occurring during the neonatal period, characterized by classical Marfan syndrome manifestations in addition to facial d...
Comprehensive, easy-to-understand information about this condition
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Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.
AI-curated news mentioning neonatal Marfan syndrome
Updated Feb 4, 2026
A personalized home-based exercise training program significantly enhances aerobic exercise capacity and health-related quality of life in children with Marfan and Loeys-Dietz syndromes. This study highlights the potential of tailored interventions in managing these rare conditions.