ABC v St George’s Healthcare NHS Trust was a missed opportunity. The case was a first opportunity for the UK courts to engage with a duty to disclose genetic risks to patients’ relatives, but Nicol J’s judgment focused on whether a duty was fair, just and reasonable and ignored issues of harm and proximity. This paper offers an answer to what the foreseeable harm, or gist damage, is in a claim of genetic nondisclosure. It considers intangible harms such as autonomy, dignity and preparedness but rejects these as formulations of harm as they fail to sufficiently recognise physical burdens of genetic conditions. The paper also explores tangible harms drawn from existing principles of tort. Loss of a chance is discussed and rejected because of ...
The completion of a rough draft of the Human Genome presents both tremendous potential for improveme...
Where there is conflict between a patient's interests in non-disclosure of their genetic information...
As an increasing number of genetic tests for specific early- and late-onset disorders move from rese...
Genetic testing can reveal information significant to patients’ relatives. This familial aspect rais...
The increasing accessibility of personal genetic information creates new challenges for the English ...
This article investigates a high-profile and ongoing dilemma for healthcare professionals (HCPs), na...
Although the subject of whether liability in negligence may arise for the nondisclose of genetic inf...
The use of 'next-generation' genetic sequencing technology that allows the sequencing of large parts...
The use of ‘next-generation’ genetic sequencing technology that allows the sequencing of large parts...
This comment analyses the recent High Court decision in Smith & Another v University of Leicester NH...
A recent English court decision raises an issue clinicians increasingly face, namely whether, when a...
In December 2019, seven women from one family underwent highly invasive surgeries based on genetic t...
Abstract: The legal duty to protect patient confidentiality is common knowledge amongst healthcare p...
The field of genetics is unique as test results reveal information about multiple individuals. When...
Although genetic disorders have been recognized for centuries, recent advances in the study of human...
The completion of a rough draft of the Human Genome presents both tremendous potential for improveme...
Where there is conflict between a patient's interests in non-disclosure of their genetic information...
As an increasing number of genetic tests for specific early- and late-onset disorders move from rese...
Genetic testing can reveal information significant to patients’ relatives. This familial aspect rais...
The increasing accessibility of personal genetic information creates new challenges for the English ...
This article investigates a high-profile and ongoing dilemma for healthcare professionals (HCPs), na...
Although the subject of whether liability in negligence may arise for the nondisclose of genetic inf...
The use of 'next-generation' genetic sequencing technology that allows the sequencing of large parts...
The use of ‘next-generation’ genetic sequencing technology that allows the sequencing of large parts...
This comment analyses the recent High Court decision in Smith & Another v University of Leicester NH...
A recent English court decision raises an issue clinicians increasingly face, namely whether, when a...
In December 2019, seven women from one family underwent highly invasive surgeries based on genetic t...
Abstract: The legal duty to protect patient confidentiality is common knowledge amongst healthcare p...
The field of genetics is unique as test results reveal information about multiple individuals. When...
Although genetic disorders have been recognized for centuries, recent advances in the study of human...
The completion of a rough draft of the Human Genome presents both tremendous potential for improveme...
Where there is conflict between a patient's interests in non-disclosure of their genetic information...
As an increasing number of genetic tests for specific early- and late-onset disorders move from rese...