Syndromic agammaglobulinaemia (Q88427): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Raro transtorno genético ligado ao X descoberto em 1952 que afeta a capacidade do corpo de combater infecções. XLA é um transtorno ligado ao X e, portanto, é muito mais comum em homens. Os pacientes com XLA não geram células B maduras, o que se manifesta como uma completa falta de anticorpos na corrente sanguínea. | |||
| description / en | description / en | ||
This is a rare X-linked genetic disorder discovered in 1952 that affects the body's ability to fight infection. XLA is an X-linked disorder, and therefore is much more common in males. XLA patients do not generate mature B cells, which manifests as a complete lack of antibodies in their bloodstream. | |||
Revision as of 14:38, 15 August 2026
This is a rare X-linked genetic disorder discovered in 1952 that affects the body's ability to fight infection. XLA is an X-linked disorder, and therefore is much more common in males. XLA patients do not generate mature B cells, which manifests as a complete lack of antibodies in their bloodstream.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1049161944 |
||
| English | Syndromic agammaglobulinaemia |
This is a rare X-linked genetic disorder discovered in 1952 that affects the body's ability to fight infection. XLA is an X-linked disorder, and therefore is much more common in males. XLA patients do not generate mature B cells, which manifests as a complete lack of antibodies in their bloodstream. |
