Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.

Clinical genetics units of hospitals occasionally receive requests from women for prenatal diagnosis for Huntington's disease when their male partners are at risk and do not want to know their genetic status for the disease. These cases raise significant legal and ethical concerns for the clini...

Full description

Bibliographic Details
Main Authors: Tassicker, R, Savulescu, J, Skene, L, Marshall, P, Fitzgerald, L, Delatycki, M
Format: Journal article
Language:English
Published: 2003
_version_ 1797080646422626304
author Tassicker, R
Savulescu, J
Skene, L
Marshall, P
Fitzgerald, L
Delatycki, M
author_facet Tassicker, R
Savulescu, J
Skene, L
Marshall, P
Fitzgerald, L
Delatycki, M
author_sort Tassicker, R
collection OXFORD
description Clinical genetics units of hospitals occasionally receive requests from women for prenatal diagnosis for Huntington's disease when their male partners are at risk and do not want to know their genetic status for the disease. These cases raise significant legal and ethical concerns for the clinical team because such prenatal tests can reveal that the woman's partner has the genetic mutation for Huntington's disease when he does not want this information and may be unprepared for it. In this paper we present clinical, legal, and ethical appraisals of this situation. We conclude that there is no easy answer to such requests and that clinical teams need to deal with them on the basis of the individual circumstances.
first_indexed 2024-03-07T01:03:04Z
format Journal article
id oxford-uuid:8a6111c1-1307-479e-b01a-a1d88ac1b1ed
institution University of Oxford
language English
last_indexed 2024-03-07T01:03:04Z
publishDate 2003
record_format dspace
spelling oxford-uuid:8a6111c1-1307-479e-b01a-a1d88ac1b1ed2022-03-26T22:31:07ZPrenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8a6111c1-1307-479e-b01a-a1d88ac1b1edEnglishSymplectic Elements at Oxford2003Tassicker, RSavulescu, JSkene, LMarshall, PFitzgerald, LDelatycki, MClinical genetics units of hospitals occasionally receive requests from women for prenatal diagnosis for Huntington's disease when their male partners are at risk and do not want to know their genetic status for the disease. These cases raise significant legal and ethical concerns for the clinical team because such prenatal tests can reveal that the woman's partner has the genetic mutation for Huntington's disease when he does not want this information and may be unprepared for it. In this paper we present clinical, legal, and ethical appraisals of this situation. We conclude that there is no easy answer to such requests and that clinical teams need to deal with them on the basis of the individual circumstances.
spellingShingle Tassicker, R
Savulescu, J
Skene, L
Marshall, P
Fitzgerald, L
Delatycki, M
Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
title Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
title_full Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
title_fullStr Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
title_full_unstemmed Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
title_short Prenatal diagnosis requests for Huntington's disease when the father is at risk and does not want to know his genetic status: clinical, legal, and ethical viewpoints.
title_sort prenatal diagnosis requests for huntington s disease when the father is at risk and does not want to know his genetic status clinical legal and ethical viewpoints
work_keys_str_mv AT tassickerr prenataldiagnosisrequestsforhuntingtonsdiseasewhenthefatherisatriskanddoesnotwanttoknowhisgeneticstatusclinicallegalandethicalviewpoints
AT savulescuj prenataldiagnosisrequestsforhuntingtonsdiseasewhenthefatherisatriskanddoesnotwanttoknowhisgeneticstatusclinicallegalandethicalviewpoints
AT skenel prenataldiagnosisrequestsforhuntingtonsdiseasewhenthefatherisatriskanddoesnotwanttoknowhisgeneticstatusclinicallegalandethicalviewpoints
AT marshallp prenataldiagnosisrequestsforhuntingtonsdiseasewhenthefatherisatriskanddoesnotwanttoknowhisgeneticstatusclinicallegalandethicalviewpoints
AT fitzgeraldl prenataldiagnosisrequestsforhuntingtonsdiseasewhenthefatherisatriskanddoesnotwanttoknowhisgeneticstatusclinicallegalandethicalviewpoints
AT delatyckim prenataldiagnosisrequestsforhuntingtonsdiseasewhenthefatherisatriskanddoesnotwanttoknowhisgeneticstatusclinicallegalandethicalviewpoints