scholarly journals Comprehensive treatment of a severe chronic periodontitis patient with anterior open bite : A case report

2008 ◽  
Vol 50 (3) ◽  
pp. 193-200
Author(s):  
Kensuke Takeuchi ◽  
Motomu Kudou ◽  
Jun Shinoda ◽  
Akemi Nishibori ◽  
Masamoto Toyoda ◽  
...  
Keyword(s):  
Case Report ◽  
Chronic Periodontitis ◽  
Open Bite ◽  
Comprehensive Treatment ◽  
Anterior Open Bite ◽  
Periodontitis Patient

Steroid-induced anterior open bite. Case report

1986 ◽  
Vol 31 (6) ◽  
pp. 455-458 ◽  
Author(s):  
Caroline H. C. Acton
Keyword(s):  
Case Report ◽  
Open Bite ◽  
Anterior Open Bite

scholarly journals Protraction Facemask Followed by Mandibular Cervical Headgear: an Alternative in the Treatment of Class III Malocclusion with Severe Anterior Open-Bite

2021 ◽  
Vol 24 (2) ◽  
Author(s):  
Matheus Pithon ◽  
Luiz Antonio Bernardes
Keyword(s):  
Case Report ◽  
Treatment Modality ◽  
Open Bite ◽  
Class Iii ◽  
Class Iii Malocclusion ◽  
Anterior Open Bite ◽  
Present Case Report ◽  
Maxilla And Mandible ◽  
Lower Arch

The present case report describes a conservative and uncommon treatment for class III malocclusion in a woman growing patient with aged eight years and four months. An unconventional treatment modality was used for the treatment of this malocclusion, reverse-pull headgear and distalisation of lower teeth using mandibular cervical headgear in the lower arch. At the end of the treatment (after 33 months), there was correction of the transversal and sagittal occlusal relationship between maxilla and mandible and correct dental intercuspation. Keywords Class III malocclusion; Open-bite; Orthodontics.

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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