Literature DB >> 23086469

Genetics and public health: the experience of a reference center for diagnosis of 22q11.2 deletion in Brazil and suggestions for implementing genetic testing.

Társis Paiva Vieira1, Ilária Cristina Sgardioli, Vera Lúcia Gil-da-Silva-Lopes.   

Abstract

Considering the prevalence of 22q11.2 deletion syndrome (22q11.2 DS) of around 1:4,000 and of palatal abnormalities in 70 % of the cases of 22q11.2 DS and taking into account the Brazilian health system and its current situation of medical genetic services, this study aims to contribute to establish strategies for genetic diagnosis. The access to genetic testing at 11 services was investigated and samples from 100 patients with palatal abnormalities and suspicion of 22q11.2 DS were sent to a reference center. Laboratorial techniques included karyotyping, fluorescence in situ hybridization (FISH), and multiplex ligation-dependent probe amplification. Costs were also calculated. Disparities among centers for genetic diagnosis were evident, with remarkable regional differences. Some of the obstacles encountered were difficulties for families to show up for medical appointments, complementary evaluations, and for the clinics to send the samples to the reference center. A conclusive diagnosis was reached for 38 % of patients. Combination of karyotyping and FISH had better laboratorial cost-effectiveness. These results might represent the reality for the investigation of other genetic conditions. Clinical and laboratorial approaches herein presented could be adapted for use under different genetic conditions in the Brazilian health system, which has relatively limited financial and human resources. Suggestions for the rational implementation of genetic testing in developing countries are presented.

Entities:  

Year:  2012        PMID: 23086469      PMCID: PMC3537976          DOI: 10.1007/s12687-012-0123-z

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  21 in total

1.  Framing genomics, public health research and policy: points to consider.

Authors:  Bartha Maria Knoppers; T Leroux; H Doucet; B Godard; C Laberge; M Stanton-Jean; S Fortin; J Cousineau; C Monardes; N Girard; L Levesque; C Durand; Y Farmer; M Dion-Labrie; M-E Bouthillier; D Avard
Journal:  Public Health Genomics       Date:  2010-04-15       Impact factor: 2.000

2.  Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome.

Authors:  L Fernández; P Lapunzina; D Arjona; I López Pajares; L García-Guereta; D Elorza; M Burgueros; M L De Torres; M A Mori; M Palomares; A García-Alix; A Delicado
Journal:  Clin Genet       Date:  2005-10       Impact factor: 4.438

Review 3.  Chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome).

Authors:  Donna M McDonald-McGinn; Kathleen E Sullivan
Journal:  Medicine (Baltimore)       Date:  2011-01       Impact factor: 1.889

4.  Local strategies to address health needs of individuals with orofacial clefts in alagoas, Brazil.

Authors:  Marshall Ítalo Barros Fontes; Lanusia Nunes Almeida; Gilberto de Oliveira Reis Junior; José Ivam Vieira Filho; Kathleen Moura Dos Santos; Filipe Silveira Dos Anjos; Ana Karolina Maia de Andrade; Carlos Guilherme Gaelzer Porciuncula; Michelline Costa de Oliveira; Rui Manoel Pereira; Tarsis Antonio Paiva Vieira; Nilma Lúcia Viguetti-Campos; Vera Lúcia Gil-da-Silva-Lopes; Isabella Lopes Monlleó
Journal:  Cleft Palate Craniofac J       Date:  2012-01-11

5.  How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

Authors:  Maija R J Kohonen-Corish; Jumana Y Al-Aama; Arleen D Auerbach; Myles Axton; Carol Isaacson Barash; Inge Bernstein; Christophe Béroud; John Burn; Fiona Cunningham; Garry R Cutting; Johan T den Dunnen; Marc S Greenblatt; Jim Kaput; Michael Katz; Annika Lindblom; Finlay Macrae; Donna Maglott; Gabriela Möslein; Sue Povey; Raj Ramesar; Sue Richards; Daniela Seminara; María-Jesús Sobrido; Sean Tavtigian; Graham Taylor; Mauno Vihinen; Ingrid Winship; Richard G H Cotton
Journal:  Hum Mutat       Date:  2010-12       Impact factor: 4.878

6.  [Birth defects in Brazil and health care: proposals for public policies in clinical genetics].

Authors:  Dafne Dain Gandelman Horovitz; Maria Helena Cabral de Almeida Cardoso; Juan Clinton Llerena; Ruben Araújo de Mattos
Journal:  Cad Saude Publica       Date:  2006-12       Impact factor: 1.632

7.  DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.

Authors:  Oliver Bartsch; Michaela Nemecková; Eduard Kocárek; Annett Wagner; Alena Puchmajerová; Maja Poppe; Katrin Ounap; Petr Goetz
Journal:  Am J Med Genet A       Date:  2003-02-15       Impact factor: 2.802

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

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

9.  Evaluation of craniofacial care outside the Brazilian reference network for craniofacial treatment.

Authors:  Isabella Lopes Monlleo; Peter Anthony Mossey; Vera Lucia Gil-da-Silva-Lopes
Journal:  Cleft Palate Craniofac J       Date:  2008-07-23

10.  How can developing countries harness biotechnology to improve health?

Authors:  Abdallah S Daar; Kathryn Berndtson; Deepa L Persad; Peter A Singer
Journal:  BMC Public Health       Date:  2007-12-03       Impact factor: 3.295

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  8 in total

1.  Diagnostic Approach to Microdeletion Syndromes Based on 22q11.2 Investigation: Challenges in Four Cases.

Authors:  Ilária C Sgardioli; Matheus de Mello Copelli; Fabíola P Monteiro; Ana P Dos Santos; Elaine Lustosa Mendes; Társis Paiva Vieira; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2017-06-24

2.  22q11.2 Deletion Syndrome: Laboratory Diagnosis and TBX1 and FGF8 Mutation Screening.

Authors:  Ilária C Sgardioli; Társis P Vieira; Milena Simioni; Fabíola P Monteiro; Vera L Gil-da-Silva-Lopes
Journal:  J Pediatr Genet       Date:  2015-03

3.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Bethina Loiseau; Li Qun Betty He; Trillium Chang; Jessica Hill; Helen Dimaras
Journal:  Genet Med       Date:  2018-08-03       Impact factor: 8.822

Review 4.  A systematic review of geographical inequities for accessing clinical genomic and genetic services for non-cancer related rare disease.

Authors:  Stephanie Best; Nada Vidic; Kim An; Felicity Collins; Susan M White
Journal:  Eur J Hum Genet       Date:  2022-01-20       Impact factor: 5.351

5.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: protocol for a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Helen Dimaras
Journal:  Syst Rev       Date:  2017-07-11

6.  Testing criteria for 22q11.2 deletion syndrome: preliminary results of a low cost strategy for public health.

Authors:  Ilária Cristina Sgardioli; Fabíola Paoli Monteiro; Paulo Fanti; Társis Paiva Vieira; Vera Lúcia Gil-da-Silva-Lopes
Journal:  Orphanet J Rare Dis       Date:  2019-06-03       Impact factor: 4.123

7.  Costs of genetic testing: Supporting Brazilian Public Policies for the incorporating of molecular diagnostic technologies.

Authors:  Rosane Paixão Schlatter; Ursula Matte; Carisi Anne Polanczyk; Patrícia Koehler-Santos; Patricia Ashton-Prolla
Journal:  Genet Mol Biol       Date:  2015-08-21       Impact factor: 1.771

8.  Cardiovascular abnormalities in patients with oral cleft: a clinical-electrocardiographic-echocardiographic study.

Authors:  Gisele C P Leite; Marcela A G Ururahy; João F Bezerra; Valéria M G D M Lima; Maria I F Costa; Sandra S C Freire; André D Luchessi; Jussara M C Maia; Maria E F Brito; Vera L Gil-da-Silva-Lopes; Adriana A Rezende
Journal:  Clinics (Sao Paulo)       Date:  2018-04-19       Impact factor: 2.365

  8 in total

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