Acrocephalosyndactyly type 3
An autosomal dominant inherited type of acrocephalosyndactyly caused by mutations in the FGFR1 or FGFR2 genes. It is characterized by early closure of the sutures between the skull bones, bulging and wide-set eyes, broad thumbs, big toes, and partial syndactyly in the hands and toes.
Disease Alternative Name
Trending Diseases
Trending Cases
- Login to View the image
X-rays are commonly used in clinical practice to diagnose fractures. Characteristics of the fracture such as the type, deformity & soft tissue / joint involvement are used to guide management. Learn & update your basic radiological approach for “Bone Fractures” & interpretation knowledge & patient care approach with this post.
Radiology Essential5 Likes8 Answers - Login to View the image
F.60yrs. LBA with swelling of legs. 3months.
Dr. Syam Sundar Patro1 Like5 Answers - Login to View the image
Check how quickly can you solve these questions using your clinical knowledge. Solve & get a chance to be the top performer. We are Live Now.
Curofy Quiz0 Like0 Answer - Login to View the image
Check out the answer for Quick Brains quiz.
Curofy Quiz0 Like0 Answer