Literature DB >> 6736220

Craniofacial morphology in the velo-cardio-facial syndrome.

M Arvystas, R J Shprintzen.   

Abstract

The velo -cardio-facial syndrome is a recently delineated congenital malformation syndrome, probably of autosomal dominant inheritance. Previous reports have concentrated on facial, oropharyngeal, cardiac, speech, language, and psychological features of this fairly common syndrome. To date, no radiographic data have been presented which might help to further delineate the syndrome, nor has there been an explanation of the characteristic facial appearance seen in this syndrome. This current study reports on cephalometric evidence of platybasia (obtuse angulation of the cranial base) in the velo -cardio-facial syndrome. The finding of platybasia adds one more phenotypic feature to the syndrome and also may help to explain the facial features of retrognathia, malar flatness, and prominence of the nasal root.

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Mesh:

Year:  1984        PMID: 6736220

Source DB:  PubMed          Journal:  J Craniofac Genet Dev Biol        ISSN: 0270-4145


  14 in total

1.  Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.

Authors:  E W Chow; D J Mikulis; R B Zipursky; L E Scutt; R Weksberg; A S Bassett
Journal:  Biol Psychiatry       Date:  1999-11-15       Impact factor: 13.382

2.  Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study.

Authors:  Marcia A Friedman; Nathanial Miletta; Cheryl Roe; Dongliang Wang; Bernice E Morrow; Wendy R Kates; Anne Marie Higgins; Robert J Shprintzen
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2011-07-18       Impact factor: 1.675

3.  Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysis.

Authors:  Rachel A Ruotolo; Nestor A Veitia; Aaron Corbin; Joseph McDonough; Cynthia B Solot; Donna McDonald-McGinn; Elaine H Zackai; Beverly S Emanuel; Avital Cnaan; Don LaRossa; Raanan Arens; Richard E Kirschner
Journal:  Cleft Palate Craniofac J       Date:  2006-07

Review 4.  Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise.

Authors:  A H Lipson; D Yuille; M Angel; P G Thompson; J G Vandervoord; E J Beckenham
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318

5.  The velo-cardio-facial (Shprintzen) syndrome. Clinical variability in eight patients.

Authors:  P Meinecke; F A Beemer; A Schinzel; T Kushnick
Journal:  Eur J Pediatr       Date:  1986-12       Impact factor: 3.183

6.  Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

Authors:  B Morrow; R Goldberg; C Carlson; R Das Gupta; H Sirotkin; J Collins; I Dunham; H O'Donnell; P Scambler; R Shprintzen
Journal:  Am J Hum Genet       Date:  1995-06       Impact factor: 11.025

7.  Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome.

Authors:  L H Seaver; J W Pierpont; R P Erickson; R L Donnerstein; S B Cassidy
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

Review 8.  Velo-cardio-facial syndrome: 30 Years of study.

Authors:  Robert J Shprintzen
Journal:  Dev Disabil Res Rev       Date:  2008

9.  Racial Variations in Velopharyngeal and Craniometric Morphology in Children: An Imaging Study.

Authors:  Lakshmi Kollara; Jamie L Perry; Suzanne Hudson
Journal:  J Speech Lang Hear Res       Date:  2016-02       Impact factor: 2.297

10.  Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics.

Authors:  E W Chow; A S Bassett; R Weksberg
Journal:  Am J Med Genet       Date:  1994-06-15
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