Open access
Aug 2026
Novel ANKRD11 Variant in a Lebanese Girl with KBG Syndrome: An 11-Year Follow-Up
This case expands the molecular spectrum of KBG syndrome and highlights the importance of genomic testing in children presenting with developmental delay, learning difficulties, and subtle dysmorphic features, particularly when the diagnosis remains uncertain during early childhood.
Maalouf George, Shaib Mohamad, Antoun Christophe et al.
· SVOA Paediatrics · 0 citations