scholarly journals Dental treatment in a hospital setting for a patient with Apert syndrome: A case report

2021 ◽  
Vol 11 (4) ◽  
pp. 1-3
Author(s):  
Martin Hogan ◽  
Isabel Pennings
Keyword(s):  
Case Report ◽  
Dental Treatment ◽  
Hospital Setting ◽  
Apert Syndrome

Providing Dental Treatment for Children in a Hospital Setting

2013 ◽  
Vol 57 (1) ◽  
pp. 163-173
Author(s):  
Elizabeth Velan ◽  
Barbara Sheller
Keyword(s):  
Dental Treatment ◽  
Hospital Setting

Ultrasound Detection of Apert Syndrome: A Case Report and Literature Review

1997 ◽  
Vol 14 (07) ◽  
pp. 427-430 ◽  
Author(s):  
Kathryn Kaufmann ◽  
Shari Baldinger ◽  
Leslie Pratt
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Apert Syndrome

Dental Treatment of Children with CATCH 22 Syndrome: Case Report

2013 ◽  
Vol 13 (1) ◽  
pp. 13
Author(s):  
Mi Sun Kim ◽  
Soo Eon Lee ◽  
Hyo Jung Ahn ◽  
Jae-Hong Park ◽  
Sung Chul Choi
Keyword(s):  
Case Report ◽  
Dental Treatment ◽  
Catch 22

scholarly journals Apert Syndrome: A Case Report and Review of Literature

2016 ◽  
Vol 06 (02) ◽  
pp. 175-184 ◽  
Author(s):  
Simon Pius ◽  
Halima Abubakar Ibrahim ◽  
Mustapha Bello ◽  
Kefas Mbaya ◽  
Jose Pwavimbo Ambe
Keyword(s):  
Case Report ◽  
Apert Syndrome ◽  
Review Of Literature

scholarly journals REFLEX EPILEPSY TRIGGERED BY DENTAL TREATMENT: A CASE REPORT

2015 ◽  
Vol 12 (12) ◽  
Author(s):  
Yeliz KILINIÇ ◽  
Berrin IŞIK ◽  
Sara SAMUR ERGÜVEN ◽  
Mustafa ARSLAN
Keyword(s):  
Case Report ◽  
Dental Treatment ◽  
Reflex Epilepsy

scholarly journals A Case Report of Apert Syndrome in a Fifty-Eight Year Old Female

2020 ◽  
Vol 3 (11) ◽  
pp. 352-354
Author(s):  
Pooja Gaur
Keyword(s):  
Case Report ◽  
Clinical Care ◽  
Open Bite ◽  
Apert Syndrome ◽  
Facial Features ◽  
Type I ◽  
Anterior Open Bite ◽  
Rare Type ◽  
Patient Reported ◽  
Hands And Feet

Defined as a rare type I acrocephalosyndactyly syndrome which is clinically characterized by dysmorphic facial features, craniosynostosis, and severe syndactyly of the hands and feet, Apert Syndrome represents an autosomal dominant inheritance which occurs due to the gene mutations in the receptors of the fibroblast growth factor. Oral lesions include tooth crowding, reduction in the size of the maxilla, impacted teeth, anterior open-bite, ectopic eruption, delayed eruption, thick gingiva and supernumerary teeth. The present case report describes a 58 year old female patient reported with the features of Apert’s syndrome such as dysmorphic facial features, occular anomalies, syndactyly and oral features. The case was referred to a specialized centre of clinical care for further treatment.

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