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Prenatal and adult presymptomatic testing for Huntington's disease
Author(s) -
Turner David R.,
Jacka Eleanor,
Kalucy Ross S.,
Burns Richard J.,
Willoughby John O.,
Crabb Rosemary,
Haan Eric A.
Publication year - 1988
Publication title -
medical journal of australia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 131
eISSN - 1326-5377
pISSN - 0025-729X
DOI - 10.5694/j.1326-5377.1988.tb93814.x
Subject(s) - huntington's disease , disease , pedigree chart , predictive testing , genetic counseling , genetic testing , medicine , test (biology) , diagnostic test , dna testing , psychology , psychiatry , clinical psychology , family medicine , pediatrics , genetics , pathology , biology , paleontology , gene
The discovery of a fragment of DNA that is linked closely to the Huntington's‐disease autosomal locus offers the opportunity for the presymptomatic diagnosis of this dominantly‐inherited neurodegenerative disorder. Presymptomatic testing will present individuals and society with difficult choices and responsibilities. A pilot adult presymptomatic test programme is under way for SA families. Presymptomatic testing requires intensive counselling both before and after the test. A form of prenatal test, which is applicable to a significant proportion of couples with one partner at risk of Huntington's disease, is available also. As this form of prenatal test does not change the risk status of the parent, less extensive counselling is required and testing is available nationally through the SA programme. It is anticipated that other states will develop their own diagnostic programmes in the near future. This article explains the basis for the test, its accuracy and the importance of obtaining DNA from key individuals in pedigrees of Huntington's disease.