Severe resting clonus caused by thyrotoxicosis in a 16‐year‐old girl with hereditary spastic paraparesis: A case report
Identifieur interne : 003B31 ( Main/Exploration ); précédent : 003B30; suivant : 003B32Severe resting clonus caused by thyrotoxicosis in a 16‐year‐old girl with hereditary spastic paraparesis: A case report
Auteurs : Terence D. Sanger [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2004-06.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Enfant.
English descriptors
- KwdEn :
- Adolescent, Case study, Child, Female, Humans, Nervous system diseases, Paraparesia, Paraparesis, Spastic (complications), Paraparesis, Spastic (genetics), Rest, Seizures (diagnosis), Seizures (etiology), Severity of Illness Index, Thyrotoxicosis (blood), Thyrotoxicosis (complications), Thyrotropin (blood), clonus, diplegia, hereditary spastic paraparesis, spasticity, spastin, thyroid, thyrotoxicosis.
- MESH :
- chemical , blood : Thyrotropin.
- blood : Thyrotoxicosis.
- complications : Paraparesis, Spastic, Thyrotoxicosis.
- diagnosis : Seizures.
- etiology : Seizures.
- genetics : Paraparesis, Spastic.
- Adolescent, Female, Humans, Rest, Severity of Illness Index.
Abstract
A 16‐year‐old girl with a history of hereditary spastic paraparesis developed the subacute onset of severe clonus and new upper‐extremity spasticity due to thyrotoxicosis. This case demonstrates the ability of hyperthyroid states to worsen symptoms of spasticity in a child with an underlying spastic disorder. It also demonstrates the importance of investigating for common systemic diseases as a cause of movement disorders even in children with underlying known genetic disorders. © 2004 Movement Disorder Society
Url:
DOI: 10.1002/mds.20015
Affiliations:
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Le document en format XML
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