scholarly journals A Rare case report of Oligodontia in the permanent dentition

2014 ◽  
Vol 13 (4) ◽  
pp. 488-491
Author(s):  
Suresh Ramamurthy
Keyword(s):  
Rare Case ◽  
Medical Science ◽  
Complex Problem ◽  
Permanent Teeth ◽  
Third Molars ◽  
Facial Disfigurement ◽  
The Third ◽  
Rare Case Report ◽  
Old Adult ◽  
And Function

Oligodontia is a rare congential disorder of dental anomalies that can occur either as an isolated finding or as part of a syndrome. It is defined as agenesis of six or more teeth excluding the third molars. It is commonly seen in permanent than in deciduous dentition. Patients suffering from oligodontia may present with complex problem such as dental and facial disfigurement. Management of those cases generally requires multidisciplinary approach to restore esthetic and function. This paper reports a rare case of oligodontia in an 18 year old adult female patient who has been missing eight permanent teeth excluding the third molars, clinically and radiographically. DOI: http://dx.doi.org/10.3329/bjms.v13i4.16048 Bangladesh Journal of Medical Science Vol.13(4) 2014 p.488-491

scholarly journals Bilateral Hypodontia of Mandibular Second Premolars and Lateral Incisors in a Nonsyndromic Patient: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 24-26
Author(s):  
Shakun Kanjani
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Permanent Teeth ◽  
Rare Occurrence ◽  
Third Molars ◽  
Missing Teeth ◽  
Dental Anomaly ◽  
Mahatma Gandhi ◽  
The Third ◽  
Rare Case Report

ABSTRACT Hypodontia is the term used to describe the developmental absence of one or more primary or permanent teeth, excluding the third molars. It is the most commonly occurring developmental dental anomaly and can be a challenge to manage clinically. Hypodontia can occur in association with syndrome or it may occur in nonsyndromic patient. Bilateral occurrence is common but it is very rare to see two bilateral congenital missing teeth in a nonsyndromic patient. This case report presents a rare occurrence of congenital bilateral missing mandibular second premolars and mandibular lateral incisors in a nonsyndromic patient. How to cite this article Agarwal N, Chaturvedy S, Marwah N, Mishra P, Kanjani S. Bilateral Hypodontia of Mandibular Second Premolars and Lateral Incisors in a Nonsyndromic Patient: A Rare Case Report. J Mahatma Gandhi Univ Med Sci Tech 2016;1(1):24-26.

Non-syndromic oligodontia in permanent dentition: a rare case report

2013 ◽  
Vol 9 (1) ◽  
Author(s):  
Parampreet Pannu ◽  
Virat Galhotra ◽  
Pooja Ahluwalia ◽  
Ramandeep Singh Gambhir
Keyword(s):  
Case Report ◽  
Self Esteem ◽  
Permanent Dentition ◽  
Permanent Teeth ◽  
Third Molars ◽  
Prosthetic Rehabilitation ◽  
Unique Case ◽  
Present Case Report ◽  
The Third ◽  
Rare Case Report

Objective: Tooth agenesis is one of the most common congenital anomalies seen in humans. Although ab¬sence of one or more teeth is common, absence of multiple teeth is rare. Oligodontia is a rare developmental anomaly, involving agenesis of six or more permanent teeth, excluding the third molars. The reported preva¬lence of oligodontia in permanent dentition is 0.14%. Oligodontia can be presented as an isolated condition or as a part of a syndrome. Discussion: The present case report highlights a unique case of non-syndromic oligodontia, with agenesis of four permanent incisors, left permanent canine and right second premolar in the mandibular arch and its management with a novel fixed functional prosthetic appliance. Conclusion: Prosthetic rehabilitation is an urgent need for these kind of patients so that they do not suffer from mastica¬tory and esthetic problems which can eventually lower the self esteem of individuals.

scholarly journals Suspected Non-Syndromic Oligodontia – A Rare Case with 13 Agenesis

2019 ◽  
Vol 53 (6) ◽  
Author(s):  
Dian Lupita Sari ◽  
Seno Pradopo ◽  
Sindy Cornelia Nelwan ◽  
Haryono Utomo ◽  
Udijanto Tedjosasongko
Keyword(s):  
Orthodontic Treatment ◽  
Rare Case ◽  
Process Management ◽  
Treatment Plan ◽  
Permanent Teeth ◽  
Third Molars ◽  
Oral Function ◽  
The Third ◽  
Congenital Condition

Oligodontia is a condition in which the patient has more than six ageneses, excluding the third molars. Whereas the absence of one tooth is quite common, oligodontia is a rare congenital condition that can happen with or without the syndrome. The condition happens due to disturbances during odontogenesis process. Management of oligodontia is a long-term process, and it involves prosthetic, restorative, and orthodontic treatment to support the oral function and esthetic of the patient. This article aims to report a rare case of agenesis of 13 permanent teeth (excluding third molars) in an 11-year-old girl and her treatment plan.

scholarly journals Nonsyndromic Oligodontia: A Rare Case Report with Review of Literature

2014 ◽  
Vol 02 (02) ◽  
pp. 109-112
Author(s):  
Puneet Bajaj ◽  
Robin Sabharwal ◽  
Sonia Joshi
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Ectodermal Dysplasia ◽  
Developmental Anomaly ◽  
Permanent Teeth ◽  
Review Of Literature ◽  
Third Molars ◽  
Missing Teeth ◽  
Rare Case Report ◽  
Oral Abnormalities

AbstractDental agenesis is the most common developmental anomaly in humans and is frequently associated with several other oral abnormalities. In the literature, some terms are used to describe missing teeth like Oligodontia, Anodontia and Hypodontia. Oligodontia is defined as the developmental absence of six teeth or more, excluding third molars. It can be isolated or as a part of a syndrome such as in ectodermal dysplasia. The present case describes agenesis of permanent teeth which are non-familial and with no apparent systemic abnormalities

Bilateral Mandibular Canine Impaction: A Rare Case Report

2009 ◽  
Vol 3 (2) ◽  
pp. 38-41
Author(s):  
Rohilla Monika ◽  
Goel Mahesh ◽  
Marwah Nikhil
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Event ◽  
Rare Condition ◽  
Permanent Tooth ◽  
Third Molars ◽  
The Third ◽  
Rare Case Report ◽  
Mandibular Canine ◽  
Orthodontic Forces

ABSTRACT Retention that is a permanent tooth which is unerupted more than a year after the normal age of eruption is a relatively rare event, except in the case of the third molars and the upper canines. We report the case of a 17 year old female presenting with bilateral mandibular canine impaction. This rare condition usually requires extraction of the involved tooth because orthodontic forces are seldom successful at erupting these teeth into their proper location. Henceforth, the canines were extracted.

scholarly journals Agenesis of Bilateral Permanent Mandibular Canine: A Rare Case Report

2016 ◽  
Vol 04 (01) ◽  
pp. 056-058
Author(s):  
Deepti Jindal ◽  
Varun Jindal ◽  
Himanshu Singh ◽  
Swati Gautam ◽  
Ishita Bhojia ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Congenital Absence ◽  
Dental Arch ◽  
Review Of Literature ◽  
Third Molars ◽  
Comprehensive Review ◽  
Rare Case Report ◽  
Mandibular Canine ◽  
Congenitally Missing

AbstractHypodontia is the congenital absence of less than six teeth because of agenesis. Congenital absence of tooth (hypodontia) from the dental arch, may occur with any tooth, most commonly being third molars, however, absence of permanent mandibular canine is rare. The absence of teeth may be unilateral or bilateral. There are reports showing unilateral occurrence of permanent mandibular canines but agenesis of bilateral mandibular canines is not well documented in the literature and comprehensive review of literature shows paucity of data pertaining to this anomaly. Here we report one such rare case of congenitally missing mandibular permanent canines bilaterally.

scholarly journals Idiopathic multiple unerupted permanent teeth: A rare case report

2014 ◽  
Vol 3 (4) ◽  
pp. 283 ◽  
Author(s):  
Sandra Vani ◽  
Anitha Nooney ◽  
KakarlaSubba Raju ◽  
Melpati Hemadri
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Permanent Teeth ◽  
Rare Case Report

scholarly journals Cerebral Coenurosis Masquerading as Malignancy: A Rare Case Report from India

2019 ◽  
Vol 10 (02) ◽  
pp. 367-370
Author(s):  
Shamila Mohamed Ali ◽  
P. Somashekara Reddy ◽  
S. Venugopal ◽  
Manmeet Chhabra ◽  
Anita Mahadevan
Keyword(s):  
Case Report ◽  
Characteristic Feature ◽  
Rare Case ◽  
Histopathological Examination ◽  
Surgical Excision ◽  
Hydatid Cysts ◽  
The Third ◽  
Rare Case Report ◽  
Cerebral Coenurosis ◽  
Cuticular Layer

ABSTRACTHuman coenurosis is a rare zoonotic disease caused by the larvae of Tinea multiceps seen in sheep-rearing countries. We report the case of a 63-year-old male who was referred to our hospital with a working diagnosis of skull base chondrosarcoma. Histopathological examination after surgical excision revealed characteristic feature of coenurus with multiple scolices invaginating from the outer cuticular layer. Coenuri are often mistaken for giant cysticercal cysts and hydatid cysts. Despite its wide prevalence in cattle, only two cases of human coenurosis are reported from India till date. We report the third case from India.

scholarly journals Extraocular Myocysticercosis Involving Levator Palpebrae Superioris-Superior Rectus Complex: A Rare case Report

2013 ◽  
Vol 4 (4) ◽  
pp. 36-39
Author(s):  
Sajid Ansari ◽  
Mukesh Kumar Gupta ◽  
Kaleem Ahmad ◽  
Kanchan Dhungel ◽  
Abhishek Kumar ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Rare Case ◽  
Medical Science ◽  
Surgical Excision ◽  
Extraocular Muscles ◽  
Science Volume ◽  
Ocular Involvement ◽  
Rare Entity ◽  
Rare Case Report ◽  
Levator Palpebrae

The ocular involvement of the cysticercosis is a rare entity involving eyelids, extraocular muscles, orbit, conjunctiva, anterior chamber, uvea, retina, vitreous and optic nerve. All the extraocular muscles are involved in myocysticercosis. Ultrasonography and Computed tomography are the imaging modalities for evaluation of ocular cysticercosis. The patients can be treated with systemic steroids and albendazole; however surgical excision is the treatment of choice. We report a rare case of extraocular myocysticercosis in nine years old boy diagnosed on ultrasonography and computed tomography. Asian Journal of Medical Science, Volume-4 (2013), Pages 36-39 DOI: http://dx.doi.org/10.3126/ajms.v4i4.8163 

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