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SCID
ADA deficiency. Recurrent viral, bacterial, fungal, and protozoal infections
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Wiskott-Aldrich Syndrome
X-linked. Triad (TIE): thrombocytopenic purpura, infections, eczema. Decreased IgM, increased IgE and IgA
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Leukocyte Adhesion Deficiency
Delayed separation of umbilicus. Recurrent bacterial infections, absent pus formation. Neutrophilia
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Chediak Higashi
Autosomal recessive. Defect in microtubular function with decreased phagocytosis. Recurrent pyogenic infections by Staph and Strep, partial albinism, peripheral neuropathy
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CGD
lack of NADPH oxidase, decreased reactive oxygen species and absent respiratory burst in neutrophils, increased susceptibility to catalase positive organisms: Staph, E.coli, Aspergillus. Negative NBT test
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