Literature DB >> 10390677

Genetically determined obesity in Prader-Willi syndrome: the ethics and legality of treatment.

A J Holland1, J Wong.   

Abstract

A central characteristic of people with Prader-Willi Syndrome (PWS) is an apparent insatiable appetite leading to severe overeating and the potential for marked obesity and associated serious health problems and premature death. This behaviour may be due to the effects of the genetic defect resulting from the chromosome 15 abnormalities associated with the syndrome. We examine the ethical and legal dilemmas that can arise in the care of people with PWS. A tension exists between a genetic deterministic perspective and that of individual choice. We conclude that the determination of the capacity of a person with PWS to make decisions about his/her eating behaviour and to control that behaviour is of particular importance in resolving this dilemma. If the person is found to lack capacity, the common law principles of acting in a person's "best interests" using the "least restrictive alternative" may be helpful. Allowing serious weight gain in the absence of careful consideration of these issues is an abdication of responsibility.

Entities:  

Keywords:  Genetics and Reproduction; Legal Approach; Mental Health Act 1983 (Great Britain); Mental Health Therapies; Professional Patient Relationship

Mesh:

Year:  1999        PMID: 10390677      PMCID: PMC479214          DOI: 10.1136/jme.25.3.230

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  5 in total

1.  Eating themselves to death: have "personal rights" gone too far in treating people with Prader-Willi syndrome?

Authors:  E M Dykens; B J Goff; R M Hodapp; L Davis; P Devanzo; F Moss; J Halliday; B Shah; M State; B King
Journal:  Ment Retard       Date:  1997-08

2.  Adults with Prader-Willi syndrome: a survey of 232 cases.

Authors:  L R Greenswag
Journal:  Dev Med Child Neurol       Date:  1987-04       Impact factor: 5.449

3.  Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Authors:  D H Ledbetter; V M Riccardi; S D Airhart; R J Strobel; B S Keenan; J D Crawford
Journal:  N Engl J Med       Date:  1981-02-05       Impact factor: 91.245

4.  Alterations in the hypothalamic paraventricular nucleus and its oxytocin neurons (putative satiety cells) in Prader-Willi syndrome: a study of five cases.

Authors:  D F Swaab; J S Purba; M A Hofman
Journal:  J Clin Endocrinol Metab       Date:  1995-02       Impact factor: 5.958

5.  Characteristics of the eating disorder in Prader-Willi syndrome: implications for treatment.

Authors:  A J Holland; J Treasure; P Coskeran; J Dallow
Journal:  J Intellect Disabil Res       Date:  1995-10
  5 in total
  2 in total

1.  Clinical management of behavioral characteristics of Prader-Willi syndrome.

Authors:  Alan Y Ho; Anastasia Dimitropoulos
Journal:  Neuropsychiatr Dis Treat       Date:  2010-05-06       Impact factor: 2.570

2.  Observed Dietary Intake in Adults with Intellectual Disability Living in Group Homes.

Authors:  Nur Hana Hamzaid; Helen T O'Connor; Victoria M Flood
Journal:  Nutrients       Date:  2019-12-22       Impact factor: 5.717

  2 in total

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