l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report

Benign hereditary chorea (BHC) is a rare autosomal dominant disease that is characterized by non-progressive chorea with early-childhood-onset, congenital hypothyroidism, and neonatal respiratory distress. Although tetrabenazine and levodopa are partly effective for chorea and drop attacks in some p...

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Veröffentlicht in:Brain & development (Tokyo. 1979) 2018-04, Vol.40 (4), p.353-356
Hauptverfasser: Shiohama, Tadashi, Ohashi, Hirofumi, Shimizu, Kenji, Fujii, Katsunori, Oba, Daiju, Takatani, Tomozumi, Kato, Mitsuhiro, Shimojo, Naoki
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Sprache:eng
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Zusammenfassung:Benign hereditary chorea (BHC) is a rare autosomal dominant disease that is characterized by non-progressive chorea with early-childhood-onset, congenital hypothyroidism, and neonatal respiratory distress. Although tetrabenazine and levodopa are partly effective for chorea and drop attacks in some patients, there is no standard treatment option. We herein describe a childhood case of BHC that presented with l-thyroxine-responsive drop attacks. A genetic analysis revealed an interstitial deletion that included two enhancer regions of NKX2-1, providing genetic confirmation of BHC. This is the first report to inform the connection between thyroid function and drop attacks in BHC. Moreover, our findings identify l-thyroxine as a therapeutic option for the management of drop attacks in BHC.
ISSN:0387-7604
1872-7131
DOI:10.1016/j.braindev.2017.12.008