Literature DB >> 15352859

Abnormal vomer development in human fetuses with isolated cleft palate.

Lene Hansen1, Dorrit Nolting, Gitte Holm, Birgit Fischer Hansen, Inger Kjaer.   

Abstract

OBJECTIVE: The aim of this study was to elucidate the prenatal human development of the vomer with emphasis on the vomeral footplate and to assess vomeral morphology in fetuses with isolated cleft palate.
MATERIAL AND METHODS: Nine human fetuses of which four were normal (menstrual age [MA] 13 to 21 weeks) and five with isolated cleft palate (14 to 19 weeks MA) were studied. Midaxial cranial tissue blocks from the fetuses were cut frontally in 4microm serial sections. Sections were stained with toluidine blue in 30% ethanol.
RESULTS: From 16 weeks MA, the vomeral footplate of normal fetuses was formed from bilateral ossifications located below a U-shaped vomeral body. Later in development, an osseous connection was found between the footplate and the vomeral body. Neither bilateral areas of ossification below the vomer nor a vomeral footplate was observed in isolated cleft palate fetuses.
CONCLUSIONS: In normal fetuses, the base or footplate of the vomeral bone appears from 16 weeks MA in frontal sections. In fetuses with isolated cleft palates, with no connection between the nasal septum and the maxillary processes, this vomeral footplate does not develop in the period observed (14 to 19 weeks MA).

Entities:  

Mesh:

Year:  2004        PMID: 15352859     DOI: 10.1597/03-058.1

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  6 in total

1.  Posteroinferior septal defect due to vomeral malformation.

Authors:  Yong Won Lee; Young Hoon Yoon; Kunho Song; Yong Min Kim
Journal:  Eur Arch Otorhinolaryngol       Date:  2019-04-25       Impact factor: 2.503

2.  Congenital Vomer Agenesis: Report of Two Cases.

Authors:  Mehdi Bakhshaee; Sherwin Tavakol; Yeganeh Teimouri
Journal:  Iran J Otorhinolaryngol       Date:  2017-05

3.  Vomer Flaps Support Velopharyngeal Competency, Fistula Free Repair, and 3D Construction of Normal Anatomy in Patients with Cleft Palate.

Authors:  Gül Schmidt; Evjenia Toubekis; Hubertus Koch; Jürgen Schlabe; Christa Hunn-Stohwasser; Benedicta Beck-Broichsitter; Max Heiland; Carsten Matuschek
Journal:  Plast Reconstr Surg Glob Open       Date:  2021-12-06

4.  Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.

Authors:  Erwin Pauws; Aya Hoshino; Lucy Bentley; Suresh Prajapati; Charles Keller; Peter Hammond; Juan-Pedro Martinez-Barbera; Gudrun E Moore; Philip Stanier
Journal:  Hum Mol Genet       Date:  2009-07-31       Impact factor: 6.150

5.  Aberrant growth of the anterior cranial base relevant to severe midface hypoplasia of Apert syndrome.

Authors:  Bong Kuen Cha; Dong Soon Choi; In San Jang; Hyun Tae Yook; Seung Youp Lee; Sang Shin Lee; Suk Keun Lee
Journal:  Maxillofac Plast Reconstr Surg       Date:  2018-12-12

6.  Topographical variations of the incisive canal and nasopalatine duct in human fetuses.

Authors:  Ji Hyun Kim; Shunichi Shibata; Hiroshi Abe; Gen Murakami; José Francisco Rodríguez-Vázquez
Journal:  Anat Cell Biol       Date:  2019-12-31
  6 in total

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