Lymphocytic Intracytoplasmic Inclusions in Infants with a Variant of Severe Combined Immunodeficiency (scid)

Abstract

SCID as a genetic disease ia inherited either as an autosomal or a sex-linked recessive with an incidence of 1:2,000,000 or 1:10,000, respectively. Over a six year period, we have identified 8 infants from a single ethnic group with a SCID rate greater than 1:3500. Three infants were born during a recent 3 month period, only one with a family history of… (More)
DOI: 10.1203/00006450-197704000-00747

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