Wiskott-Aldrich syndrome (Q52912): Difference between revisions
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A síndrome de Wiskott-Aldrich é uma rara deficiência imunológica hereditária com herança recessiva ligada ao cromossomo X (Xp11.22-p11.23), caracterizada pela associação de trombocitopenia com plaquetas de pequeno tamanho, eczema e infecções de repetição. A deficiência ocorre precocemente da infância, durante a primeira década e geralmente antes dos 3 anos de idade. | |||
| description / en | description / en | ||
Wiskott-Aldrich syndrome is a rare hereditary immune deficiency with recessive inheritance linked to the X chromosome (Xp11.22-p11.23), characterised by the association of thrombocytopenia with small-sized platelets, eczema and repeated infections. The deficiency occurs early in childhood, during the first decade and usually before the age of 3 years. | |||
Revision as of 00:15, 14 August 2026
Wiskott-Aldrich syndrome is a rare hereditary immune deficiency with recessive inheritance linked to the X chromosome (Xp11.22-p11.23), characterised by the association of thrombocytopenia with small-sized platelets, eczema and repeated infections. The deficiency occurs early in childhood, during the first decade and usually before the age of 3 years.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_168952525 |
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| English | Wiskott-Aldrich syndrome |
Wiskott-Aldrich syndrome is a rare hereditary immune deficiency with recessive inheritance linked to the X chromosome (Xp11.22-p11.23), characterised by the association of thrombocytopenia with small-sized platelets, eczema and repeated infections. The deficiency occurs early in childhood, during the first decade and usually before the age of 3 years. |
