Pakistan Journal of Medicine and Dentistry 2013, Vol. 1 (01) 2-11Pakistan Journal of Medicine and Dentistry 2015, Vol. 4 (01): p-p 74 CASE REPORT Hernia Bhesham Kumar Shahani

A Guide to the Diagnosis and Treatment of Apert SyndromeA Guide to the Diagnosis and Treatment of Apert Syndrome Having a child born with Apert syndrome may feel over- whelming.

Apert syndromeApert syndrome Description Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure

IJCPD Apert’s Syndrome 1Gudipaneni Ravi Kumar, 2Mandapati Jyothsna, 3Syed Basheer Ahmed, 4Ketham Reddy Sree Lakshmi IJCPD 1,2Assistant Professor, 3Associate Professor,

Apert syndrome: A case report and review of the literature Tuba Tulay Koca Department of Physical Medicine and Rehabilitation, Malatya State Hospital, Malatya, Turkey ABSTRACT

Ref: 2019F1683 © GOSH NHS Foundation Trust, December 2019 Page 1 of 3 Apert syndrome: information for families Apert syndrome is a type of complex craniosynostosis named

Background Information many ways. AS impacts the growth of the bones of the head and face. The skull is made of bony plates. They are held together in babies and children

©1997 Erlanger Health System Tennessee Craniofacial Center 1(800) 418-3223 fashion across the posterior aspect of the skull. Premature fusion or synostosis of this suture

untitledCopyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. A third report of Apert syndrome in association with diaphragmatic hernia Badr H. Sobaiha and

Iranian Rehabilitation Journal 92 Masoud Gharib University of Social Welfare and Rehabilitation Sciences, Pediatric Neurorehabilitation Research Center, Tehran, Iran Nazila