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Reduction of striatal glucose metabolism in McLeod choreoacanthocytosis
McLeod syndrome is a distinct form of neuroacanthocytosis. Its defining feature is the depression of erythrocyte Kell antigens. The underlying X chromosomal mutations cause a dysfunction of an erythrocyte membrane protein Kx. A choreatic movement disorder with caudate atrophy in CT and MRI has been...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Group
2001
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1737311/ https://ncbi.nlm.nih.gov/pubmed/11254778 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp.70.4.517 |
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