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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