Academic
Publications
Apert syndrome- a case report

Apert syndrome- a case report,Muddu Gopi Krishna,Saritha Purushothaman,Senior Resident

Apert syndrome- a case report  
BibTex | RIS | RefWorks Download
Apert syndrome is a rare congenital disorder which is a part of Acrocephalosyndactyly syndromes. It is characterized by craniosynostosis, symmetrical syndactyly of hands and feet. We present a case of Apert syndrome with clinical features of brachycephaly, proptosis, flat forehead, low set ears with syndactyly of hands and feet.
Published in 2012.
Cumulative Annual
View Publication
The following links allow you to view full publications. These links are maintained by other sources not affiliated with Microsoft Academic Search.