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Say's syndrome

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A familial syndrome characterized by multiple abnormalities, a chemotactic defect, and transient hypogammaglobulinaemia. Inheritance is probably autosomal recessive.


  • B. Say, et al:
    Microcephaly, short stature, and developmental delay with a chemotactic defect and hypogammaglobulinaemia in two brothers.
    Journal of Medical Genetics, London, 1986; 23: 355-359.

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