Patient Data
Age: Child
From the case:
Apert syndrome
{"current_user":null,"step_through_annotations":true,"access":{"can_edit":false,"can_download":true,"can_toggle_annotations":true,"can_feature":false,"can_examine_pipeline_reports":false,"can_pin":false},"extraPropsURL":"/studies/10827/annotated_viewer_json?iframe=true\u0026lang=us"}
Multifocal syndactyly and symphalangism.
Case Discussion
Apert syndrome (type I acrocephalosyndactyly) is characterized by complex syndactyly. Symphalangism is often also present.