McLeod syndrome (Q99666): Difference between revisions
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Transtorno de neuroacantocitose ligado ao X, causado por mutações no gene XK que codifica os antígenos Kell das hemácias. Caracterizada por degeneração do caudato e putâmen levando a coreia progressiva, neuropatia periférica e miopatia com aumento no nível de creatina quinase sérica. | |||
| description / en | description / en | ||
An X linked disorder of neuroacanthocytosis that is caused by mutations in the XK gene coding for the Kell antigens red blood cells. Characterized by degeneration of the caudate and putamen leading to progressive chorea, peripheral neuropathy, and myopathy with increase in serum creatine kinase level. | |||
Revision as of 16:20, 16 August 2026
An X linked disorder of neuroacanthocytosis that is caused by mutations in the XK gene coding for the Kell antigens red blood cells. Characterized by degeneration of the caudate and putamen leading to progressive chorea, peripheral neuropathy, and myopathy with increase in serum creatine kinase level.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_463702616 |
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| English | McLeod syndrome |
An X linked disorder of neuroacanthocytosis that is caused by mutations in the XK gene coding for the Kell antigens red blood cells. Characterized by degeneration of the caudate and putamen leading to progressive chorea, peripheral neuropathy, and myopathy with increase in serum creatine kinase level. |
