Aldrich syndrome


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Aldrich syndrome

[′ȯl·drich ‚sin‚drōm]
(medicine)
A recessive, sex-linked disease characterized by a complex of symptoms, including eczematoid dermatitis, thrombocytopenia, black stool, and a deficiency of immune globulins.
References in periodicals archive ?
Isolation of a novel gene mutated in Wiskott Aldrich Syndrome.
In mid-August, Holly Campbell gave birth to another son, Rylan, who also has Wiskott Aldrich syndrome.
Among those attending was 16-month-old Jack Hayhoe, who has the rare Whiskott Aldrich Syndrome.
They later found the baby had the rare Wiskott Aldrich Syndrome, a condition which affects only a handful of people in the country.
Eleven-month-old Jack Hayhoe, from Hoylake, was diagnosed with Wiskott Aldrich Syndrome when he was only a few months old.
They later found the baby had the rare Wiskott Aldrich Syndrome - a condition which affects just a handful of people in the country.