Literature DB >> 10464611

Discovery of children's carrier status for recessive genetic disease: some ethical issues.

D S Davis1.   

Abstract

Knowledge of one's carrier status for recessive genetic diseases is useful primarily in making marital and reproductive decisions. These decisions are peculiarly the private domain of the young adults who are dating, mating, and forming new families. The privacy of these decisions may be compromised when parents know the carrier status of their children. Thus, the practice of sharing that information with the parents of fetuses, babies, and minor children ought to be discouraged, out of respect for the autonomy and privacy of these children when they become adults.

Entities:  

Keywords:  Genetics and Reproduction

Mesh:

Year:  1998        PMID: 10464611     DOI: 10.1089/gte.1998.2.323

Source DB:  PubMed          Journal:  Genet Test        ISSN: 1090-6576


  5 in total

1.  Guidelines for genetic testing of healthy children.

Authors: 
Journal:  Paediatr Child Health       Date:  2003-01       Impact factor: 2.253

Review 2.  Les tests et le dépistage génétiques chez les enfants.

Authors:  Aideen M Moore; Julie Richer
Journal:  Paediatr Child Health       Date:  2022-07-18       Impact factor: 2.600

Review 3.  Genetic testing and screening in children.

Authors:  Aideen M Moore; Julie Richer
Journal:  Paediatr Child Health       Date:  2022-07-18       Impact factor: 2.600

4.  Effort required to contact primary care providers after newborn screening identifies sickle cell trait.

Authors:  Stephanie A Christopher; Jenelle L Collins; Michael H Farrell
Journal:  J Natl Med Assoc       Date:  2012 Nov-Dec       Impact factor: 1.798

Review 5.  The ethical framework for performing research with rare inherited neurometabolic disease patients.

Authors:  Viviana Giannuzzi; Hugo Devlieger; Lucia Margari; Viveca Lena Odlind; Lamis Ragab; Cinzia Maria Bellettato; Francesca D'Avanzo; Christina Lampe; Linda Cassis; Elisenda Cortès-Saladelafont; Ángels Garcia Cazorla; Ivo Barić; Ljerka Cvitanović-Šojat; Ksenija Fumić; Christine I Dali; Franco Bartoloni; Fedele Bonifazi; Maurizio Scarpa; Adriana Ceci
Journal:  Eur J Pediatr       Date:  2017-01-16       Impact factor: 3.183

  5 in total

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