Apert syndrome- a case report

Journal Title: International Journal of Medical and Health Sciences - Year 2012, Vol 1, Issue 1

Abstract

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.

Authors and Affiliations

Muddu Gopi Krishna, Saritha Purushothaman

Keywords

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  • EP ID EP39647
  • DOI -
  • Views 377
  • Downloads 0

How To Cite

Muddu Gopi Krishna, Saritha Purushothaman (2012). Apert syndrome- a case report. International Journal of Medical and Health Sciences, 1(1), -. https://europub.co.uk/articles/-A-39647