Novel genetic disease claim struck out: A and M v University Hospitals of Leicester NHS Trust (High Court, 15 April 2016 Judge McKenna)

Mr X suffers from a genetic disease known as AMN, which adversely impacts upon the white matter of the brain. A and B are, or were, second cousins of X. A suffers from Adrenoleukodystrophy (ALD) the childhood version of AMN, as did B until his death on 26 April 2012. Both A and B were diagnosed with...

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Veröffentlicht in:	Clinical risk 2015-11, Vol.21 (6), p.128-129
1. Verfasser:	Mead, John
Format:	Artikel
Sprache:	eng
Schlagworte:	Disease Genetic disorders
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description	Mr X suffers from a genetic disease known as AMN, which adversely impacts upon the white matter of the brain. A and B are, or were, second cousins of X. A suffers from Adrenoleukodystrophy (ALD) the childhood version of AMN, as did B until his death on 26 April 2012. Both A and B were diagnosed with ALD in 2006. In brief, it was alleged that the condition suffered by X should has been diagnosed by the trust earlier and that this would, in turn, have led to an earlier diagnosis of the condition in both A and B, leading to significantly better outcomes for both of them.
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source	Applied Social Sciences Index & Abstracts (ASSIA); SAGE Complete
subjects	Disease Genetic disorders
title	Novel genetic disease claim struck out: A and M v University Hospitals of Leicester NHS Trust (High Court, 15 April 2016 Judge McKenna)
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