Literature DB >> 8773902

The search for hemizygosity at 22qll in patients with isolated cleft palate.

R Mingarelli1, M C Digilio, A Mari, F Amati, L Standoli, A Giannotti, G Novelli, B Dallapiccola.   

Abstract

The striking association between oral clefting and the velocardio-facial syndrome (VCFS), a common disorder pathogenetically related to 22q11 deficiency, has prompted the search for this deletion in a group of patients with isolated cleft palate. (CP). Thirty-three patients with posterior CP and 5 with complete CP were included in this study, together with 12 patients with a clinical diagnosis of VCFS. Standard and high resolution chromosome analysis was performed, providing normal results. Southern blotting followed by densitometric analysis and fluorescent in situ hydridization of region 22q11 showed no single case of deletion among the isolated CP patients, while deficiency was found in 10 of 12 VCFS patients. These results demonstrate that hemizygosity at 22q11 is not increased in isolated CP.

Entities:  

Mesh:

Year:  1996        PMID: 8773902

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


  4 in total

Review 1.  22q11 deletion syndrome: a genetic subtype of schizophrenia.

Authors:  A S Bassett; E W Chow
Journal:  Biol Psychiatry       Date:  1999-10-01       Impact factor: 13.382

2.  Defining new guidelines for screening the 22q11.2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature.

Authors:  Fabíola P Monteiro; Társis P Vieira; Ilária C Sgardioli; Miriam C Molck; Ana Paula Damiano; Josiane Souza; Isabella L Monlleó; Marshall I B Fontes; Agnes C Fett-Conte; Têmis M Félix; Gabriela F Leal; Erlane M Ribeiro; Claudio E M Banzato; Clarissa de R Dantas; Iscia Lopes-Cendes; Vera Lúcia Gil-da-Silva-Lopes
Journal:  Eur J Pediatr       Date:  2013-02-26       Impact factor: 3.183

3.  22q11 deletion syndrome in adults with schizophrenia.

Authors:  A S Bassett; K Hodgkinson; E W Chow; S Correia; L E Scutt; R Weksberg
Journal:  Am J Med Genet       Date:  1998-07-10

4.  Prevalence of 22q11.2 microdeletion syndrome in Iranian patients with cleft palate.

Authors:  Narges Nouri; Mehrdad Memarzadeh; Mansoor Salehi; Nayereh Nouri; Rokhsareh Meamar; Mahdiyeh Behnam; Fatemeh Derakhshandeh; Tahereh Kashkoolinejad; Hossein Abdali
Journal:  Adv Biomed Res       Date:  2016-12-27
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.