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Literature DB >> 16491420

Is genetic testing of healthy pre-symptomatic children with possible Alport syndrome ethical?

Lawrence Copelovitch, Bernard S Kaplan.

Abstract

Entities: Disease Species

Mesh：

Year: 2006 PMID： 16491420 DOI： 10.1007/s00467-005-0003-4

Source DB: PubMed Journal: Pediatr Nephrol ISSN： 0931-041X Impact factor: 3.714

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12 in total

Review 1. A practical primary care approach to hematuria in children.

Authors: S C Diven; L B Travis
Journal: Pediatr Nephrol Date: 2000-01 Impact factor: 3.714

2. Canadian experience with predictive testing for Huntington disease: lessons for genetic testing centers and policy makers.

Authors: M A Chapman
Journal: Am J Med Genet Date: 1992-02-15

3. The clinical significance of asymptomatic gross and microscopic hematuria in children.

Authors: Jerry Bergstein; Jeffrey Leiser; Sharon Andreoli
Journal: Arch Pediatr Adolesc Med Date: 2005-04

4. X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

Authors: Jean Philippe Jais; Bertrand Knebelmann; Iannis Giatras; Mario DE Marchi; Gianfranco Rizzoni; Alessandra Renieri; Manfred Weber; Oliver Gross; Kai-Olaf Netzer; Frances Flinter; Yves Pirson; Christine Verellen; Jörgen Wieslander; Ulf Persson; Karl Tryggvason; Paula Martin; Jens Michael Hertz; Cornelis Schröder; Marek Sanak; Sarka Krejcova; Maria Fernanda Carvalho; Juan Saus; Corinne Antignac; Hubert Smeets; Marie Claire Gubler
Journal: J Am Soc Nephrol Date: 2000-04 Impact factor: 10.121

10. Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors.

Authors:
Journal: Am J Hum Genet Date: 1995-11 Impact factor: 11.025

2 in total

1. Diagnosis of Alport syndrome without biopsy?

Authors: Marie Claire Gubler
Journal: Pediatr Nephrol Date: 2006-12-02 Impact factor: 3.714

Review 2. Alport syndrome--insights from basic and clinical research.

Authors: Jenny Kruegel; Diana Rubel; Oliver Gross
Journal: Nat Rev Nephrol Date: 2012-11-20 Impact factor: 28.314

2 in total

Is genetic testing of healthy pre-symptomatic children with possible Alport syndrome ethical?

Review 1. A practical primary care approach to hematuria in children.

2. Canadian experience with predictive testing for Huntington disease: lessons for genetic testing centers and policy makers.

3. The clinical significance of asymptomatic gross and microscopic hematuria in children.

4. X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

5. The importance of non-invasive genetic analysis in the initial diagnostics of Alport syndrome in young patients.

6. Persistent familial hematuria in children and the locus for thin basement membrane nephropathy.

7. Meta-analysis of genotype-phenotype correlation in X-linked Alport syndrome: impact on clinical counselling.

Review 8. Genetic testing for renal diseases: medical and ethical considerations.

9. Limited evaluation of microscopic hematuria in pediatrics.

10. Points to consider: ethical, legal, and psychosocial implications of genetic testing in children and adolescents. American Society of Human Genetics Board of Directors, American College of Medical Genetics Board of Directors.

1. Diagnosis of Alport syndrome without biopsy?

Review 2. Alport syndrome--insights from basic and clinical research.