Literature DB >> 8378162

Triple-X syndrome accompanied by single maxillary central incisor: case report.

M Miura1, N Kato, H Kojima, H Oguchi.   

Abstract

Facial, oral, and dental findings of an 11-year-old girl with XXX syndrome are reported. Clinical examination reveals midfacial hypoplasia, congenital absence of teeth, and solitary maxillary central incisors both in primary and permanent dentitions.

Entities:  

Mesh：

Year:  1993        PMID： 8378162

Source DB:  PubMed          Journal:  Pediatr Dent        ISSN： 0164-1263            Impact factor:   1.874


  4 in total

Review 1.  Solitary median maxillary central incisor syndrome (SMMCI) with congenital nasal puriform aperture stenosis: literature review and case report with comprehensive dental treatment and 14 years follow-up.

Authors:  N N Lygidakis; K Chatzidimitriou; N Petrou; N A Lygidakis
Journal:  Eur Arch Paediatr Dent       Date:  2013-06-18

2.  Sella Turcica Shape in Fragile X Syndrome.

Authors:  Reinhard E Friedrich
Journal:  In Vivo       Date:  2021 Nov-Dec       Impact factor: 2.155

Review 3.  Solitary median maxillary central incisor (SMMCI) syndrome.

Authors:  Roger K Hall
Journal:  Orphanet J Rare Dis       Date:  2006-04-09       Impact factor: 4.123

4.  Solitary Median Maxillary Central Incisor Syndrome: An Exploration of the Pathogenic Mechanism.

Authors:  Jie Li; Dandan Liu; Yang Liu; Chenying Zhang; Shuguo Zheng
Journal:  Front Genet       Date:  2022-01-24       Impact factor: 4.599
  4 in total

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