Literature DB >> 25091626

Management of a child with severe hypodontia in the mixed dentition stage of development.

H J Tong1, J F Tahmassebi.   

Abstract

BACKGROUND: Severe hypodontia is a condition characterized by developmental absence of six or more teeth and affects 0.14-0.3% of the overall population. Hypodontia can have a marked psychosocial effect and functional implications for a growing child. CASE REPORT: A 10-year-old girl with a medical history of hypothyroidism and repaired spinal bifida was referred to the Leeds Dental Institute as she was becoming increasingly concerned about her appearance. On clinical examination, the patient had severe wear of her over-retained maxillary primary central incisors, microdontia of mandibular anterior teeth (32, 34, 41, 42, 43), and loss of anterior vertical dimension. Radiographic examination revealed that the patient had 11 missing permanent teeth (14, 13, 12, 11, 21, 22, 23, 24, 31, 35, 44), an ectopic mandibular left canine and taurodontism of the permanent molars. TREATMENT: Management of the patient included an intensive preventive programme with placement of fissure sealants; scaling of calculus deposition on microdont teeth; composite resin reconstruction of microdont teeth; fabrication of removable partial overdentures tailored aesthetically to match the patient's age; orthodontic consultation and monitoring for the eruption of ectopic canine and permanent dentition. The patient and her parents reported marked improvement in self-esteem following dental treatment. FOLLOW-UP: After 2 years of follow-up, a new pair of dentures were made and designed to allow ease of eruption of the existing permanent dentition. All permanent teeth have erupted. The patient is ready for further assessment and planning for future orthodontic and restorative/implant treatment.
CONCLUSION: This case illustrates the essential role of the paediatric dentist in the management of hypodontia in the mixed dentition stage.

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Year:  2014        PMID: 25091626     DOI: 10.1007/s40368-014-0137-9

Source DB:  PubMed          Journal:  Eur Arch Paediatr Dent        ISSN: 1818-6300


  19 in total

1.  MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.

Authors:  M J van den Boogaard; M Dorland; F A Beemer; H K van Amstel
Journal:  Nat Genet       Date:  2000-04       Impact factor: 38.330

2.  The interdisciplinary management of hypodontia: orthodontics.

Authors:  N E Carter; T J Gillgrass; R S Hobson; N Jepson; J G M Eechan; F S Nohl; J H Nunn
Journal:  Br Dent J       Date:  2003-04-12       Impact factor: 1.626

3.  A meta-analysis of the prevalence of dental agenesis of permanent teeth.

Authors:  Bart J Polder; Martin A Van't Hof; Frans P G M Van der Linden; Anne M Kuijpers-Jagtman
Journal:  Community Dent Oral Epidemiol       Date:  2004-06       Impact factor: 3.383

4.  Further studies of a model for the etiology of anomalies of tooth number and size in humans.

Authors:  A H Brook; C Elcock; M H al-Sharood; H F McKeown; K Khalaf; R N Smith
Journal:  Connect Tissue Res       Date:  2002       Impact factor: 3.417

Review 5.  Prevalence of dental anomalies in nonsyndromic individuals with cleft lip and palate: a systematic review and meta-analysis.

Authors:  Patricia Nivoloni Tannure; Cristiana Aroeira G R Oliveira; Lucianne Cople Maia; Alexandre R Vieira; José Mauro Granjeiro; Marcelo de Castro Costa
Journal:  Cleft Palate Craniofac J       Date:  2011-07-08

Review 6.  Prevalence of hypodontia and developmental malformation of permanent teeth in Saudi Arabian schoolchildren.

Authors:  S al-Emran
Journal:  Br J Orthod       Date:  1990-05

Review 7.  The interdisciplinary management of hypodontia: restorative dentistry.

Authors:  N J Jepson; F S Nohl; N E Carter; T J Gillgrass; J G Meechan; R S Hobson; J H Nunn
Journal:  Br Dent J       Date:  2003-03-22       Impact factor: 1.626

8.  A controlled study of the association of various dental anomalies with hypodontia of permanent teeth.

Authors:  P Y Lai; W K Seow
Journal:  Pediatr Dent       Date:  1989-12       Impact factor: 1.874

9.  Gene defect in hypodontia: exclusion of EGF, EGFR, and FGF-3 as candidate genes.

Authors:  S Arte; P Nieminen; S Pirinen; I Thesleff; L Peltonen
Journal:  J Dent Res       Date:  1996-06       Impact factor: 6.116

10.  A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.

Authors:  Laura Lammi; Katri Halonen; Sinikka Pirinen; Irma Thesleff; Sirpa Arte; Pekka Nieminen
Journal:  Eur J Hum Genet       Date:  2003-11       Impact factor: 4.246

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