Literature DB >> 15578625

Velocardiofacial syndrome with single central incisor.

Snehlata Oberoi1, Karin Vargervik.   

Abstract

Three siblings and their mother are reported who all had cytogenetically proven velocardiofacial syndrome (VCFS). One boy had normal dental and craniofacial findings, except for an increased cranial base angle. His sister had only one central incisor in the maxilla. One central incisor had also been missing in the primary dentition. She had no labial frenulum present. Cephalometry showed a small maxillary unit length indicating mild maxillary hypoplasia, an increased anterior face height, steep mandibular plane angle, retruded chin, and a large cranial base angle. Dental measurements showed retroclined lower incisors and increased interincisal angle. A second sister had a cleft of the secondary palate. All permanent teeth were present with the exception of a missing central incisor in the lower jaw: the single lower central incisor was situated in the midline. Her cephalometry showed similar findings as in her sister. All three siblings required palate surgery for speech. Mother was not available for detailed dental and other oral investigations. A single maxillary central incisor has previously been reported in VCFS, but to our knowledge a single central incisor in the mandible has not been reported previously in this entity.

Entities:  

Mesh:

Year:  2005        PMID: 15578625     DOI: 10.1002/ajmg.a.30434

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  10 in total

Review 1.  Developmental disorders of the dentition: an update.

Authors:  Ophir D Klein; Snehlata Oberoi; Ann Huysseune; Maria Hovorakova; Miroslav Peterka; Renata Peterkova
Journal:  Am J Med Genet C Semin Med Genet       Date:  2013-10-04       Impact factor: 3.908

2.  Tbx1 regulates oral epithelial adhesion and palatal development.

Authors:  Noriko Funato; Masataka Nakamura; James A Richardson; Deepak Srivastava; Hiromi Yanagisawa
Journal:  Hum Mol Genet       Date:  2012-02-27       Impact factor: 6.150

Review 3.  Craniofacial Phenotypes and Genetics of DiGeorge Syndrome.

Authors:  Noriko Funato
Journal:  J Dev Biol       Date:  2022-05-13

4.  Solitary Median Maxillary Central Incisor due to Nasal Pyriform Aperture Stenosis in Fetus: The First Prenatal Ultrasound Case Report.

Authors:  Florent Fuchs; Manon Chadelle; Guillaume Captier; Olivier Prodhomme; Jean Michel Faure
Journal:  Int J Clin Pediatr Dent       Date:  2020 May-Jun

Review 5.  Solitary median maxillary central incisor (SMMCI) syndrome.

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

Review 6.  Update on 13 Syndromes Affecting Craniofacial and Dental Structures.

Authors:  Theodosia N Bartzela; Carine Carels; Jaap C Maltha
Journal:  Front Physiol       Date:  2017-12-14       Impact factor: 4.566

7.  Dental Findings in Patients With Non-surgical Hypoparathyroidism and Pseudohypoparathyroidism: A Systematic Review.

Authors:  Jane Hejlesen; Line Underbjerg; Hans Gjørup; Agnes Bloch-Zupan; Tanja Sikjaer; Lars Rejnmark; Dorte Haubek
Journal:  Front Physiol       Date:  2018-06-19       Impact factor: 4.566

8.  Solitary median maxillary central incisor syndrome: A rare entity.

Authors:  Anurag Negi; Amita Negi; Megha Mohanan
Journal:  J Oral Maxillofac Pathol       Date:  2020-09-09

9.  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

10.  Platybasia in 22q11.2 deletion syndrome is not correlated with speech resonance.

Authors:  Nicole E Spruijt; Moshe Kon; Aebele B Mink van der Molen
Journal:  Arch Plast Surg       Date:  2014-07-15
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.