Late-onset neurological symptoms in thalidomide-exposed subjects: a study of an Australasian cohort
Background and purpose Thalidomide was marketed for the treatment of morning sickness and resulted in foetal death and physical deformities. The exact mechanism of action of thalidomide in its teratogenicity is still actively debated in the literature. Methods This study reviewed 16 of the confirmed...
Saved in:
Published in | European journal of neurology Vol. 20; no. 3; pp. 509 - 514 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.03.2013
John Wiley & Sons, Inc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Background and purpose
Thalidomide was marketed for the treatment of morning sickness and resulted in foetal death and physical deformities. The exact mechanism of action of thalidomide in its teratogenicity is still actively debated in the literature.
Methods
This study reviewed 16 of the confirmed Australasian victims of in utero exposure to thalidomide who now presented with new‐onset neurological symptoms in the fourth and fifth decades.
Results
Clinical neurological examination and neurophysiological investigations revealed that new symptoms were due in part to compressive neuropathies, often exacerbated by the adaptations made to accommodate the disability and poor mobility arising from the limb deformities. Other subjects were found to have musculoskeletal symptoms due to compensatory postures employed to perform tasks of daily living.
Conclusions
The study provides no evidence of ongoing loss of neurons or late reactivated neural degeneration and no evidence of a generalized peripheral neuropathy. Rather, the development of new symptoms in subjects can be explained by compressive neuropathies and compensatory postures employed to perform tasks of daily living. |
---|---|
Bibliography: | istex:3366E46DE1899ED808E0197AA6691FEBDA104E89 ark:/67375/WNG-F4XF7B3G-W ArticleID:ENE12005 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 1351-5101 1468-1331 1468-1331 |
DOI: | 10.1111/ene.12005 |