Loading...
Loading...
Disclaimer: Informational only โ not medical advice. AI hypotheses are not clinically validated. Medic Oath is for informational and educational purposes only โ not medical advice. AI-generated hypotheses have not been clinically validated. Always consult a qualified healthcare professional. Privacy ยท Terms
A rare chromosomal anomaly clinically characterized by mild to severe intellectual disability, severe developmental delay (psychomotor and speech development), hypotonia with tendency to later develop progressive hypertonia, and characteristic facial features. The main congenital anomalies associated include central nervous system (CNS) malformations such as hypoplasia/agenesis of the corpus callosum (80%), skeletal abnormalities such as scoliosis/kyphosis or dislocated hips (60%), and congenita
No hypotheses generated for this disease yet.
The autonomous pipeline will investigate this disease when evidence emerges.