Literature DB >> 20809043

Oral manifestations in Apert syndrome: case presentation and a brief review of the literature.

Andrada Soancă1, Diana Dudea, H Gocan, Alexandra Roman, B Culic.   

Abstract

BACKGROUND: The present paper describes the oral manifestations in a 16-year-old boy previously diagnosed with Apert syndrome. PATIENT AND METHODS: The extraoral and intraoral pathological findings were recorded. The following intraoral parameters were recorded: plaque and calculus deposits, dental caries, periodontal status, malpositions, and occlusion. For the upper anterior teeth, dental shade was recorded, using a dental spectrophotometer. The corresponding diagnostics were established. A treatment plan was established and discussed with the child's parents.
RESULTS: The dysmorphic characters were obvious, including acrocephaly, prominent forehead, hypoplastic midface, hypertelorism, short nose. The intraoral features revealed a bifid uvula and Byzantine-arch palate associated with lateral swellings of the palatine processes, one on either side of the middle miming a pseudocleft in the midline. Heavy dental plaque, dental calculus, congestion and swelling of the gingiva and periodontal pseudopockets associated with anterior teeth were recorded. Dental caries on anterior and posterior teeth were present. Severe maxillary dental crowding associated with the rotation of central incisors and the palatal position of second bicuspids and the malposition of the mandibular anterior teeth were observed. No intrinsic discoloration of the dental structure was recorded. Severe anterior and posterior open bite and crossbite were observed. Other signs were represented by syndactyly involving partial fusion of the fingers and toes. Also, mild mental deficiency was recorded.
CONCLUSIONS: The information and the strong motivation of the parents regarding the necessity of the treatment and the extensive use of home prevention methods are essential to control oral conditions in these patients.

Entities:  

Mesh:

Year:  2010        PMID: 20809043

Source DB:  PubMed          Journal:  Rom J Morphol Embryol        ISSN: 1220-0522            Impact factor:   1.033


  6 in total

Review 1.  The molecular and cellular basis of Apert syndrome.

Authors:  Chao Liu; Yazhou Cui; Jing Luan; Xiaoyan Zhou; Jinxiang Han
Journal:  Intractable Rare Dis Res       Date:  2013-11

2.  Apert Syndrome: Dental management considerations and objectives.

Authors:  Line Droubi; Mohannad Laflouf; Yasser Alsayed Tolibah; John C Comisi
Journal:  J Oral Biol Craniofac Res       Date:  2022-04-28

3.  Review of Etiology of Posterior Open Bite: Is There a Possible Genetic Cause?

Authors:  Wei Huang; Bo Shan; Brittany S Ang; Jennifer Ko; Richard D Bloomstein; Thomas J Cangialosi
Journal:  Clin Cosmet Investig Dent       Date:  2020-06-25

Review 4.  Cleft Palate in Apert Syndrome.

Authors:  Delayna Willie; Greg Holmes; Ethylin Wang Jabs; Meng Wu
Journal:  J Dev Biol       Date:  2022-08-11

5.  Apert syndrome: a case report.

Authors:  Saba Khan; Laxmikanth Chatra; Prashanth Shenai; Km Veena
Journal:  Int J Clin Pediatr Dent       Date:  2012-12-05

Review 6.  Dental approach for Apert syndrome in children: a systematic review.

Authors:  A-S López-Estudillo; M-A Rosales-Bérber; S Ruiz-Rodríguez; A Pozos-Guillén; M-Á Noyola-Frías; A Garrocho-Rangel
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2017-11-01
  6 in total

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