McLeod syndrome (Q99666): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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. |
Statements
CID11:ID_463702616
0 references
dki-india-ID_463702616
0 references
Concluído
0 references
15 August 2026
0 references
