→ Kabuki Syndrome (KDM6A mutation)

→ Kabuki Syndrome (KDM6A mutation)

Back to Previous Kabuki Syndrome (KDM6A mutation) Kabuki syndrome is a rare, multisystem disorder characterized by multiple abnormalities including distinctive facial features, growth delays, varying degrees of intellectual disability, skeletal abnormalities, and...
→ Kabuki Syndrome (KDM6A mutation)

→ Keipert Syndrome

Back to Previous Keipert Syndrome (Nasodigitoacoustic Syndrome) A rare multiple congenital anomalies syndrome characterized by facial dysmorphism (hypertelorism, broad and high nasal bridge, depressed nasal ridge, short columella, underdeveloped maxilla, and prominent...
→ Kabuki Syndrome (KDM6A mutation)

→ Kennedy’s Disease

Back to Previous Kennedy Disease Kennedy disease is a rare, X-linked slowly progressive neuromuscular disorder. Kennedy disease is typically an adult-onset disease, where symptoms occur mainly between the ages of 20 and 50. The disease is characterized by symptoms...