Literature DB >> 20640335

[The importance of genetic counseling at sickle cell anemia].

Cínthia Tavares Leal Guimarães1, Gabriela Ortega Coelho.   

Abstract

The genetic counseling has the purpose of guiding people through a conscientious and balanced decision making process regarding procreation, helping them to understand how the hereditary succession can contribute for the occurrence or risk of recurrence of genetic illnesses, as it is the case of the sickle cell anemia. This type of anemia is the most prevalence hereditary illness in Brazil and has clinical complications that can harm the development, the quality of life and lead to death. The present article has the objective to clarify the importance of the genetic counseling for the anemia carriers or falciform trace, aiming at to point out the main characteristics of this illness, its complications and how the diagnosis is made. The study was based on the bibliographical method, looking for studies that deal with this type of anemia and genetic counseling, relating them with guidelines and data from the Health Ministry. Based on the found data, we infer the importance of genetic counseling for the individuals who present the heterozygote form of sickle cell anemia - the falcemic trace - and highlight the need to implement precocious diagnostics programs and genetic and social/psychological orientation for those with the disease or falciform trace.

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Year:  2010        PMID: 20640335     DOI: 10.1590/s1413-81232010000700085

Source DB:  PubMed          Journal:  Cien Saude Colet        ISSN: 1413-8123


  6 in total

1.  Critical analysis of the neonatal screening program for hemoglobinopathies.

Authors:  Raphaela Martins Muniz Moreira; Isabeth da Fonseca Estevão; Débora Gusmão Melo
Journal:  Rev Bras Hematol Hemoter       Date:  2011

2.  Implementation of Indigenous Electronic Medical Record System to Facilitate Care of Sickle Cell Disease Patients in Chhattisgarh.

Authors:  Mona Choubey; Hrishikesh Mishra; Khushboo Soni; Pradeep Kumar Patra
Journal:  J Clin Diagn Res       Date:  2016-02-01

3.  Mortality by sickle cell disease in Brazil.

Authors:  Giovanna Abadia Oliveira Arduini; Letícia Pinto Rodrigues; Alessandra Bernadete Trovó de Marqui
Journal:  Rev Bras Hematol Hemoter       Date:  2016-10-21

4.  A model of genetic guidance for hemoglobinopathy patients and laboratory diagnosis of family members as educational and preventive measures.

Authors:  Tatiana Dela-Sávia Ferreira; Adriana Sousa Freire; Elisângela de Paula Silveira-Lacerda; Marco Túlio Antônio García-Zapata
Journal:  Rev Bras Hematol Hemoter       Date:  2012

5.  Follow-up of children with hemoglobinopathies diagnosed by the Brazilian Neonatal Screening Program in the State of Pernambuco.

Authors:  Ana Caroline Novaes Soares; Isabella Chagas Samico; Aderson Silva Araújo; Marcos André C Bezerra; Betânia Lucena Domingues Hatzlhofer
Journal:  Rev Bras Hematol Hemoter       Date:  2014-05-28

6.  SPATIAL DISTRIBUTION OF NEWBORNS WITH SICKLE CELL TRAIT IN SERGIPE, BRAZIL.

Authors:  Débora Cristina Fontes Leite; Rosana Cipolotti; Ricardo Queiroz Gurgel; Paulo Ricardo Saquete Martins Filho; Gabriel Dantas Lopes
Journal:  Rev Paul Pediatr       Date:  2020-03-09
  6 in total

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