Wiskott-Aldrich syndrome (Q52912): Difference between revisions

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Latest 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
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.