Wiskott-Aldrich syndrome (Q52912): Difference between revisions
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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 |
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| 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. |
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CID11:ID_168952525
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