Patient Data
Age: 7 years
Gender: Male
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/24735/annotated_viewer_json?lang=us"}
Very abnormal fingers bilaterally.
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/7722/annotated_viewer_json?lang=us"}
Brachycephalic skull.
Note: This case has been tagged as "legacy" as it no longer meets image preparation and/or other case publication guidelines.
Case Discussion
The Apert syndrome (also known as type I acrocephalosyndactyly) is a syndrome predominantly characterized by skull and limb malformations.
Unable to process the form. Check for errors and try again.