Medical Definition of Aldrich syndrome
1.
An sex-linked (X chromosome) genetic disorder occurring in male children that is characterised by thrombocytopenia, eczema, melena and susceptibility to bacterial infections. Death often occurs from severe haemorrhage or overwhelming sepsis.
Inheritance: sex-linked (X chromosome).
(27 Sep 1997)
Lexicographical Neighbors of Aldrich Syndrome
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